Dch Nerve Pain Relief Spray, Lidocaine 4%, Menthol 1%

Dch Nerve Pain Relief Spray, Lidocaine 4%, Menthol 1%
SPL v2
SPL
SPL Set ID 00db480a-e510-a64d-e063-6394a90a4695
Route
TOPICAL
Published
Effective Date 2023-06-08
Document Type 34390-5 HUMAN OTC DRUG LABEL

Drug Facts

Composition & Product

Active Ingredients
Lidocaine (4 g) Menthol (1 g)
Inactive Ingredients
Arnica Montana Flower Propylene Glycol Alcohol Chamaemelum Nobile Flower Eucalyptus Oil Aloe Vera Leaf Medium-chain Triglycerides

Identifiers & Packaging

Marketing Status
OTC MONOGRAPH DRUG Active Since 2023-03-24

Description

Lidocaine 4%, Menthol 1%


Medication Information

Warnings and Precautions

For external use only.

Flammable--Keep away from fire or flame.

Do not use if you have had an allergic reaction to lidocaine or other local anesthetics, on large areas of he body or on cut, irritated, blistered or swollen skin, on puncture wounds, for more than one week without consulting a doctor.

When using this product only use as directed, avoid contact with eyes and mucous membranes, rare cases of serious burns have been reported with products of this type, do not apply to wounds or damaged, broken, or irritated skin, do not bandage tightly or apply local heat (such as heating pads) or a medicated path to the area of use, a transient burning sensation may occur upon application but generally disappears in several days, avoid applying into skin folds.

Stop use and ask a doctor if condition worsens, severe burning sensation, redness, rash or irritation develops, symptoms persist for more than 7 days or clear up and occur again within a few days, you experience signs of skin injury, such as pain, swelling, or blistering where the product was applied.

.

Indications and Usage

Temporarily relieves minor pain

Dosage and Administration

When practical, cleanse the affected area with mild soap and warm water, Rinse thoroughly and gently pat dry. Spray affected area. Wash hands after applying. Adults and children 2 years of age and older, apply externally to the affected area up to 6 times a day. Children under 12 years of age: consult a doctor.

Description

Lidocaine 4%, Menthol 1%

Section 50565-1

If swallowed, get medical help or contact a Poison Control Center right away.

Section 51727-6

Alcohol denat., caprylic/capric triglyceride, propylene glycol, arnica montana flower extract, anthemis nobilis flower oil, aloe barbadensis leaf extract, eucalyptus globulus leaf oil.

Section 51945-4

Section 55105-1



Topical anesthetic, Topical analgesic

Section 55106-9

Lidocaine 4%, Menthol 1%


Structured Label Content

Indications and Usage (34067-9)

Temporarily relieves minor pain

Dosage and Administration (34068-7)

When practical, cleanse the affected area with mild soap and warm water, Rinse thoroughly and gently pat dry. Spray affected area. Wash hands after applying. Adults and children 2 years of age and older, apply externally to the affected area up to 6 times a day. Children under 12 years of age: consult a doctor.

Warnings and Precautions (34071-1)

For external use only.

Flammable--Keep away from fire or flame.

Do not use if you have had an allergic reaction to lidocaine or other local anesthetics, on large areas of he body or on cut, irritated, blistered or swollen skin, on puncture wounds, for more than one week without consulting a doctor.

When using this product only use as directed, avoid contact with eyes and mucous membranes, rare cases of serious burns have been reported with products of this type, do not apply to wounds or damaged, broken, or irritated skin, do not bandage tightly or apply local heat (such as heating pads) or a medicated path to the area of use, a transient burning sensation may occur upon application but generally disappears in several days, avoid applying into skin folds.

Stop use and ask a doctor if condition worsens, severe burning sensation, redness, rash or irritation develops, symptoms persist for more than 7 days or clear up and occur again within a few days, you experience signs of skin injury, such as pain, swelling, or blistering where the product was applied.

.

Section 50565-1 (50565-1)

If swallowed, get medical help or contact a Poison Control Center right away.

Section 51727-6 (51727-6)

Alcohol denat., caprylic/capric triglyceride, propylene glycol, arnica montana flower extract, anthemis nobilis flower oil, aloe barbadensis leaf extract, eucalyptus globulus leaf oil.

Section 51945-4 (51945-4)

Section 55105-1 (55105-1)



Topical anesthetic, Topical analgesic

Section 55106-9 (55106-9)

Lidocaine 4%, Menthol 1%


Advanced Ingredient Data


Raw Label Data

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