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OTC products · Product label record

NeuroNesic Pain Relieving Cream drug information

CAPSAICIN
Blaine Labs Inc. · CUTANEOUS

Product NDC: 63347-999

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Source label information, not individualized medical advice. This record applies to the product and labeler shown below. Compare the exact formulation, strength and country with your package and the current source label.
Generic nameCAPSAICIN
Labeler / manufacturerBlaine Labs Inc.
RouteCUTANEOUS
Drug classDrug class not supplied in source label
Product NDC63347-999
Label effective date2026-09-04

Official product label reference

NeuroNesic Pain Relieving Cream — Blaine Labs Inc.

This page contains 8 source sections for CAPSAICIN, cutaneous route. Label set 7107c13d-bf59-4c0a-84fe-725a9fca2691, version 1.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

USES ■ For temporary relief from minor aches and pains of sore muscles and joints associated with arthritis pain, simple backache, strains and sprains ■ Provides warming pain relief

Purpose

Purpose ............... Topical Analgesic
Dosage and administration — label text
Directions ■ Adults and children 18 years of age and older: Apply to affected area no more than 3 to 4 times daily. Wash hands with soap and water after each use. ■ Children under 18 years of age: do not use, consult a physician.
Warnings
Warnings - for external use only Do not use: ■ on wounds or damaged skin with a heating pad ■ if allergic to capsicum or chili peppers When using this produc : ■ test on a small area of skin before first use to check for skin sensitivity ■ avoid contact with eyes or mucous membranes ■ do not bandage tightly ■ do not expose area to direct heat or direct sunlight ■ a slight burning sensation may occur upon application and generally disappears within several days Stop use and ask a physician if : ■ condition worsens ■ redness is present ■ symptoms persist for more than 7 days or clear up and occur again within a few days ■ excessive skin irritation develops
Active ingredient
DRUG FACTS Active Ingredients Capsaicin ............ 0.1%
Child safety
Keep out of reach of children. If swallowed, get medical help or contact a poison control center (1-800-222-2222) immediately
Other safety information
Other Information Store in a cool, dry place at 15º-30ºC (59º-86ºF).
Inactive ingredient
Inactive Ingredients Alkyl (C12-15) Benzoate, Caprylyl Glycol, Carica Papaya (Papaya) Fruit Extract, Carthamus Tinctorius (Safflower) Seed Oil, Cetyl Alcohol, Dimethicone, Disodium EDTA, Emulsifying Wax, Ethylhexylglycerin, Glycerin, Glyceryl Stearate, Hexylene Glycol, Hydrogenated Polydecene, Hydroxyethyl Cellulose, PEG-100 Stearate, Phenoxyethanol, Propylene Glycol, Purified Water, Sodium Lactate, Sodium Polyacrylate, Trideceth-6, Xanthan Gum

Official sources and product identifiers

Substances listed: CAPSAICIN

RxNorm identifiers: 646333

Package NDC codes

63347-999-01

Further research and background

These are external searches for related information. Research, encyclopedia and news articles have not been imported into this product record.

Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.