Neuromed 7 Topical Pain Relief Cream

Neuromed 7 Topical Pain Relief Cream
SPL v15
SPL
SPL Set ID f199f56b-d971-4cf8-834d-babb5c2ff81a
Route
TOPICAL
Published
Effective Date 2024-07-25
Document Type 34390-5 HUMAN OTC DRUG LABEL

Drug Facts

Composition & Product

Inactive Ingredients
Arnica Montana Flower Water C13-14 Isoparaffin Sodium Chondroitin Sulfate (porcine; 5500 Mw) Emu Oil Diethylene Glycol Monoethyl Ether Ethylhexylglycerin Glucosamine Sulfate Isopropyl Palmitate Melaleuca Alternifolia Leaf Dimethyl Sulfone Phenoxyethanol Propylene Glycol Stearic Acid Trolamine

Identifiers & Packaging

Marketing Status
OTC MONOGRAPH DRUG Active Since 2013-08-15
Description

Lidocaine HCL 4.0% w/w

Purpose

External Anesthetic

Medication Information

Purpose

External Anesthetic

Description

Lidocaine HCL 4.0% w/w

Uses

For temporary relief of pain and itching due to minor skin irritations.

Section 50565-1

- ​Keep out of reach of children.​  If product is swallowed, get medical help or contact a Poison Control Center right away.

Section 50566-9

- ​Stop use and ask a doctor​if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days.  Discontinue use.

Section 50570-1

- ​Do not use​in large quantities, particularly over raw surfaces or blistered areas.

Warnings

- For external use only.

- Avoid contact with eyes.

Directions

For adults and children two-years or older: Apply to affected area not more than 3 or 4 times daily.  Children under 2 years of age: consult a physician.

Product Label

Active Ingredients

Lidocaine HCL 4.0% w/w

​other Information

Protect this product from excessive heat and direct sun.

​inactive Ingredients

Aqua (Deionized Water), Arnica Montana Floweri Extract, C13-14 Isoparaffin, Chondroitin Sulfate, Emu Oil, Ethoxydiglycol, Ethylhexylglycerin, Glucosamine Sulfate, Isopropyl Palmitate, Laureth-7, Melaleuca Alternifolia (Tea Tree) Oil, Methylsulfonylmenthane (MSM), Phenoxyethanol, Polyacrylamide, Propylene Glycol, Stearic Acid, Triethanolamine.

​questions Or Comments?

FDA Registered: NDC No 54723-175-22

[email protected]

Structured Label Content

Uses

For temporary relief of pain and itching due to minor skin irritations.

Section 50565-1 (50565-1)

- ​Keep out of reach of children.​  If product is swallowed, get medical help or contact a Poison Control Center right away.

Section 50566-9 (50566-9)

- ​Stop use and ask a doctor​if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days.  Discontinue use.

Section 50570-1 (50570-1)

- ​Do not use​in large quantities, particularly over raw surfaces or blistered areas.

Purpose

External Anesthetic

Warnings

- For external use only.

- Avoid contact with eyes.

Directions

For adults and children two-years or older: Apply to affected area not more than 3 or 4 times daily.  Children under 2 years of age: consult a physician.

Product Label (Product label)

Active Ingredients

Lidocaine HCL 4.0% w/w

​other Information (​Other Information)

Protect this product from excessive heat and direct sun.

​inactive Ingredients (​Inactive Ingredients)

Aqua (Deionized Water), Arnica Montana Floweri Extract, C13-14 Isoparaffin, Chondroitin Sulfate, Emu Oil, Ethoxydiglycol, Ethylhexylglycerin, Glucosamine Sulfate, Isopropyl Palmitate, Laureth-7, Melaleuca Alternifolia (Tea Tree) Oil, Methylsulfonylmenthane (MSM), Phenoxyethanol, Polyacrylamide, Propylene Glycol, Stearic Acid, Triethanolamine.

​questions Or Comments? (​Questions or Comments?)

FDA Registered: NDC No 54723-175-22

[email protected]

Advanced Ingredient Data

Raw Label Data

All Sections (JSON)

Additional Information

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Source: dailymed · Ingested: 2026-02-15T12:03:20.599307 · Updated: 2026-03-14T23:13:37.162375