Dendracin neurodendraxcin lotion

Active ingredients

Methyl Salicylate 30%

Menthol 10%

Capsaicin 0.025%


Topical Analgesic


For temporary relief of mild pain due to muscular strain, arthritis, and simple back pain. Does not cure any disease.


For external use only. Do not use in eyes, mouth, on mucous membranes, or genitals. Do not tightly bandage. Do not use with heating pad. Do not use with other topical pain products.

Keep away from children.


Use only as directed. Shake before each use. Prior to first use, rub small amount to check for sensitivity. Gently rub over painful areas. Dry before contact with clothes or bedding to avoid staining. Wash hands after use. Do not use more than 4 times daily or if pregnant or nursing. If swallowed, call poison control. If placed into eyes, rinse with cold water and call a doctor.

Do not use:

On cuts or infected skin, on children less than 12 years old, in large amounts, especially over raw or blistered skin, if allergic to any ingredients, PABA, aspirin products, or sulfa.

Store below 90F/32C.

Stop use and ask a physician:

For severe undiagnosed pain. If pain worsens or persist for more than 7 days. If pain clears up and then recurs in a few days. If itching or rash occurs.

Inactive ingredients:

Water, benzocaine, glyceryl stearate, PEG 100 stearate, stearic acid, cetyl alcohol, propylene glycol, dimethyl sulfoxide, triethanolamine, poloxamer 407, aloe barbadensis gel, borage oil, ammonium acryloyldimethyltaurate, zingiber officinale root extract, methylparaben, propylparaben, soya lecithin, DMDM hydantoin, sodium stearoyl glutamate.

Spl unclassified section

Manufactured for Physicians' Science and Nature, Inc.

220 Newport Center Drive 11-634, Newport Beach, CA 92660

Made in the USA

Patent Pending

Repackaged by:

Proficient Rx LP

Thousand Oaks, CA 91320

Ingredients and appearance - Product information

Dendracin neurodendraxcin lotion- Methyl salicylate, menthol and capsaicin

Product information

Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC: 63187-136
Route of Administration Topical

Active Ingredient/Active Moiety

Ingredient Name Strength
Methyl salicylate ( UNII: LAV5U5022Y)( Salicylic acid - UNII: O414PZ4LPZ ) 18 gin 60 mL
Menthol, unspecified form ( UNII: L7T10EIP3A)( Menthol - UNII: L7T10EIP3A ) 6 gin 60 mL
Capsaicin ( UNII: S07O44R1ZM)( Capsaicin - UNII: S07O44R1ZM ) 0.015 gin 60 mL

Inactive Ingredients

Ingredient Name Code
Water ( UNII: 059QF0KO0R)
Benzocaine ( UNII: U3RSY48JW5)
Glyceryl monostearate ( UNII: 230OU9XXE4)
Peg-100 stearate ( UNII: YD01N1999R)
Stearic acid ( UNII: 4ELV7Z65AP)
Propylene glycol ( UNII: 6DC9Q167V3)
Cetyl alcohol ( UNII: 936JST6JCN)
Dimethyl sulfoxide ( UNII: YOW8V9698H)
Poloxamer 407 ( UNII: TUF2IVW3M2)
Aloe vera leaf ( UNII: ZY81Z83H0X)
Borage seed oil ( UNII: F8XAG1755S)
Ammonio methacrylate copolymer type a ( UNII: 8GQS4E66YY)
Ginger ( UNII: C5529G5JPQ)
Lecithin, soybean ( UNII: 1DI56QDM62)
Methylparaben ( UNII: A2I8C7HI9T)
Propylparaben ( UNII: Z8IX2SC1OH)
Dmdm hydantoin ( UNII: BYR0546TOW)
Sodium stearoyl glutamate ( UNII: 65A9F4P024)
Trolamine ( UNII: 9O3K93S3TK)

Product Characteristics

Marketing Information

Marketing Category Application Number or Monograph Citation Territorial Authority Marketing Start Date
OTC monograph not final part348 USA

Labeler - Proficient Rx LP( 079196022)


Name ID/FEI Business Operations
Proficient Rx LP 079196022 RELABEL( 63187-136), REPACK( 63187-136)

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