Drugs Similar to 2677 FIRST AID BURN CREAM

2677 FIRST AID BURN

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By Substance

Drugs sharing the same substance name

0.5% LIDOCAINE BURN RELIEF LIDOCAINE HYDROCHLORIDE
UNIVERSAL DISTRIBUTION CENTER LLC FDA OTC

Uses for the temporary relief of pain and itching associated with • minor burns • sunburn • minor cuts • scrapes • insect bites • minor skin irritations

0.5% LIDOCAINE HCl 0.5% LIDOCAINE HCL
HF ACQUISITION CO LLC, DBA HEALTHFIRST FDA Rx Only

Lidocaine Hydrochloride Injection, USP is a sterile, nonpyrogenic solution of lidocaine hydrochloride in water for injection for parenteral administration in various concentrations with characteristics as follows: Multiple-dose vials contain 0.1% of methylparaben added as preservative. May contain sodium hydroxide and/or hydrochloric acid for pH adjustment. The pH is 6.5 (5.0 to 7.0). See HOW SUPPLIED section for various sizes and strengths. Lidocaine is a local anesthetic of the amide type. Lidocaine Hydrochloride, USP is chemically designated 2-(diethylamino)-N-(2,6-dimethylphenyl)-acetamide monohydrochloride monohydrate, a white powder freely soluble in water. The molecular weight is 288.82. It has the following structural formula: The semi-rigid vial used for the plastic vials is fabricated from a specially formulated polyolefin. It is a copolymer of ethylene and propylene. The safety of the plastic has been confirmed by tests in animals according to USP biological standards for plastic containers. The container requires no vapor barrier to maintain the proper drug concentration. DESCRIPTION STRUCTURE

1168 1168 BURN
DYNAREX CORPORATION FDA OTC

Use(s) For the temporary relief of pain associated with minor burns

1438 DynaSoap ANTIBACTERIAL HAND SOAP
DYNAREX CORPORATION FDA OTC

Use Cleaning and antiseptic cleansing of hands and skin.

1% LIDOCAINE HCI 1% LIDOCAINE HCI
HF ACQUISITION CO LLC, DBA HEALTHFIRST FDA Rx Only

Lidocaine Hydrochloride Injection, USP is a sterile, nonpyrogenic solution of lidocaine hydrochloride in water for injection for parenteral administration in various concentrations with characteristics as follows: Multiple-dose vials contain 0.1% of methylparaben added as preservative. May contain sodium hydroxide and/or hydrochloric acid for pH adjustment. The pH is 6.5 (5.0 to 7.0). See HOW SUPPLIED section for various sizes and strengths. Lidocaine is a local anesthetic of the amide type. Lidocaine Hydrochloride, USP is chemically designated 2-(diethylamino)-N-(2,6-dimethylphenyl)-acetamide monohydrochloride monohydrate, a white powder freely soluble in water. The molecular weight is 288.82. It has the following structural formula: The semi-rigid vial used for the plastic vials is fabricated from a specially formulated polyolefin. It is a copolymer of ethylene and propylene. The safety of the plastic has been confirmed by tests in animals according to USP biological standards for plastic containers. The container requires no vapor barrier to maintain the proper drug concentration. DESCRIPTION STRUCTURE

1% LIDOCAINE HCI, 2% LIDOCAINE HCI 1% LIDOCAINE HCI
HF ACQUISITION CO LLC, DBA HEALTHFIRST FDA Rx Only

Lidocaine Hydrochloride Injection, USP is a sterile, nonpyrogenic solution of lidocaine hydrochloride in water for injection for parenteral administration in various concentrations with characteristics as follows: Multiple-dose vials contain 0.1% of methylparaben added as preservative. May contain sodium hydroxide and/or hydrochloric acid for pH adjustment. The pH is 6.5 (5.0 to 7.0). See HOW SUPPLIED section for various sizes and strengths. Lidocaine is a local anesthetic of the amide type. Lidocaine Hydrochloride, USP is chemically designated 2-(diethylamino)-N-(2,6-dimethylphenyl)-acetamide monohydrochloride monohydrate, a white powder freely soluble in water. The molecular weight is 288.82. It has the following structural formula: The semi-rigid vial used for the plastic vials is fabricated from a specially formulated polyolefin. It is a copolymer of ethylene and propylene. The safety of the plastic has been confirmed by tests in animals according to USP biological standards for plastic containers. The container requires no vapor barrier to maintain the proper drug concentration. DESCRIPTION STRUCTURE

2.0% LIDOCAINE BURN LIDOCAINE HYDROCHLORIDE
UNIVERSAL DISTRIBUTION CENTER LLC FDA OTC

​Uses Temporary pain relief associated with minor burns

2% LIDOCAINE HCI 2% LIDOCAINE HCI
HF ACQUISITION CO. LLC, DBA HEALTH FIRST FDA Rx Only

Lidocaine Hydrochloride Injection, USP is a sterile, nonpyrogenic solution of an antiarrhythmic agent administered intravenously by either direct injection or continuous infusion. It is available in various concentrations with the following characteristics: May contain sodium hydroxide and/or hydrochloric acid for pH adjustment. Injections containing 10 mg/mL (1%) contain sodium chloride 7 mg and injections containing 20 mg/mL (2%) lidocaine hydrochloride contain sodium chloride 6 mg to adjust tonicity. Single-dose solutions contain no preservative and unused portions must be discarded after use. Lidocaine Hydrochloride, USP is chemically designated 2-(Diethylamino)-2',6'-acetoxylidide monohydrochloride monohydrate, a white powder freely soluble in water. The molecular formula is C14H22N2O • HCl • H2O. The molecular weight is 288.82. It has the following structural formula: The semi-rigid vial used for the plastic vials is fabricated from a specially formulated polyolefin. It is a copolymer of ethylene and propylene. The safety of the plastic has been confirmed by tests in animals according to USP biological standards for plastic containers. The container requires no vapor barrier to maintain the proper drug concentration. The plastic syringe is molded from a specially formulated polypropylene. Water permeates from inside the container at an extremely slow rate which will have an insignificant effect on solution concentration over the expected shelf life. Solutions in contact with the plastic container may leach out certain chemical components from the plastic in very small amounts; however, biological testing was supportive of the safety of the syringe material. Availability Structure

2% LIDOCAINE HCI 2% LIDOCAINE HCI
HF ACQUISITION CO LLC, DBA HEALTHFIRST FDA Rx Only

Lidocaine Hydrochloride Injection, USP is a sterile, nonpyrogenic solution of lidocaine hydrochloride in water for injection for parenteral administration in various concentrations with characteristics as follows: Multiple-dose vials contain 0.1% of methylparaben added as preservative. May contain sodium hydroxide and/or hydrochloric acid for pH adjustment. The pH is 6.5 (5.0 to 7.0). See HOW SUPPLIED section for various sizes and strengths. Lidocaine is a local anesthetic of the amide type. Lidocaine Hydrochloride, USP is chemically designated 2-(diethylamino)-N-(2,6-dimethylphenyl)-acetamide monohydrochloride monohydrate, a white powder freely soluble in water. The molecular weight is 288.82. It has the following structural formula: The semi-rigid vial used for the plastic vials is fabricated from a specially formulated polyolefin. It is a copolymer of ethylene and propylene. The safety of the plastic has been confirmed by tests in animals according to USP biological standards for plastic containers. The container requires no vapor barrier to maintain the proper drug concentration. DESCRIPTION STRUCTURE

2XL Mega Rolls Sanitizing Wipes BENZALKONIUM CHLORIDE

Uses to sanitize hands without requiring water or a rinse kills 99.9% of most common germs

4% Lidocaine Pain Relief Patch LIDOCAINE PAIN RELIEF
XUZHOU LANTING PHARMACEUTICAL CO., LTD FDA OTC

Uses Uses For temporary relief of minor aches & pains of muscles & joints associated with: simple backache arthritis strains bruises sprains

4% lidocaine plus 1% menthol Pain Relief Patch PAIN RELIEF PAIN RELIEF STRIP
XUZHOU LANTING PHARMACEUTICAL CO., LTD FDA OTC

Uses Uses For temporary relief of pain

4x Medicated Gum Cream BENZOCAINE

for the temporary relief of pain due to minor irritation or injury of the mouth and gums first aid to help prevent infection in minor oral irritation

4X Medicated Severe Toothache and Gum Cream BENZOCAINE

Warnings Methemoglobinemia warning: use of this product may cause methemoglobinemia, a serious condition that must be treated promptly because it reduces teh amount of oxygen carried in blood. This can occur even if you have used this product before. Stop use and seek immediate medical attention if you or a child in your care develops: * pale, gray, or blue colored skin (cyanosis) * headache * rapid heart rate * shortness of breath * dizziness or lightheadedness * fatigue or lack of energy Allergy alert do not use this product if you have a history of allergy to local anesthetics such as procaine, butacaine, benzocaine, or other "caine" anesthetics Do not use * more than directed * for more than 7 days unless told to do so by a dentist or doctor * for teething * in children under 2 years of age Stop use and ask a doctor if * swelling, rash or fever develops * irritation, pain or redness persists or worsens * symtoms do not improve in 7 days * allergic reaction occurs Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

4x Medicated Severe Toothache and Gum Gel BENZALKONIUM CHLORIDE

Directions Directions •cut open tip of tube on score mark • adults and children 2 years of age and older: apply a small amount of product to the cavity and around the gum surrounding the teeth. Use up to 4 times daily or as directed by children under 12 years of age should be supervised in the use of this product • children under a dentist or doctor • 2 years of age: do not use

4X Medicated Severe Toothache and Gum Gel BENZOCAINE

Warnings Methemoglobinemia warning: use of this product ay cause methemoglobinemia, a serious condition that must be treated promptly because it reduces the amount of oxygen carried in teh blood. This can occur even if you have used this product before. Stop use and seek immediate medical attention if you or a child in your care develops: * pale, gray, or blue colored skin (cyanosis) * headache * rapid heart rate * shortness of breath * dizziness or lightneadedness * fatigue or lack of energy Allergy Alert do not use this product if you have a history of allergy to local anesthetics such as procaine, butacaine, benzocaine or other "caine" anesthetics Do not use * more than directed * for more than 7 days unless told to do so by a dentist or doctor * for teething * in children under 2 years of age Stop use and ask a doctor if * swelling, rash or fever develops * irritation, pain or redness persists or worsens * symptoms do not improve in 7 days * allergic reaction occurs Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

4x Medicated Toothache and Gum Cream BENZOCAINE

Use for the temporary relief of pain due to toothaches * to help protect against infection or minor oral irritation

4x Medicated Toothache and Gum Cream BENZOCAINE

Use * for the temporary relief of pain due to toothaches * to help prevent against infection of minor oral irritation

4x Medicated Toothache and Gum Cream BENZOCAINE

Use for the temporary relief of pain due to toothaches * to help protect against infection of minor oral irritation

4x Medicated Toothache and Gum Cream BENZOCAINE

Use for the temporary relief of pain due to minor irritation of injury of the mouth and gums first aid to help prevent infection in miro oral irritation

By Active Ingredients

Drugs sharing any active ingredients

First Aid Burn Cream FIRST AID BURN
FRONT LINE SAFETY FDA OTC

Use(s) • For the temporary relief of pain and itching associated with: • Sunburn • Minor burns • Insect bites • Minor skin irritations • Cuts • Scrapes

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