DENDRACIN NEURODENDRAXCIN

Manufacturer
DirectRx
Effective date
2023-10-06
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 21:24:55

Label at a glance#

ProductDENDRACIN NEURODENDRAXCIN
Active ingredientMETHYL SALICYLATE, CAPSAICIN, MENTHOL
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Methyl Salicylate 30%
Menthol 10%
Capsaicin 0.025%

OTC - PURPOSE SECTION

Topical Analgesic

WARNINGS SECTION

For external use only. Do not use in eyes, mouth, on mucous membranes, or genitals. Do not allow treated skin to contact infants or pets. Do not tightly bandage. Do not use with heating pad. Do not use with other topical pain products. May stain furniture.

INDICATIONS & USAGE SECTION

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

OTC - STOP USE SECTION

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.

OTC - DO NOT USE SECTION

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 90°F/32°C.

INACTIVE INGREDIENT SECTION

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 Physician’s Science and Nature Inc.
220 Newport Center Drive 11-634, Newport Beach, CA 92660

Made in the USA
Patent Pending

DOSAGE & ADMINISTRATION SECTION

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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

680680

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

680-04680-04

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
61919-680-02ML - Milliliter61919-68084a18a7c-4b72-481f-b738-cf08316d3f7112021-10-08
61919-680-04ML - Milliliter61919-6803c0539e1-21b7-4e2a-9f7a-711d52a2bed712021-10-08
27495-014-02ML - Milliliter27495-014c650ba41-26d0-4a0c-8aa5-e506bad4bc3812012-07-24
27495-014-04ML - Milliliter27495-01457cee12b-4811-4fbd-9fa3-e71c5e5af99a12012-07-24

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61919-68061919-680-02, 61919-680-04
27495-014

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Dendracin NeurodendraxcinMETHYL SALICYLATE, MENTHOL AND CAPSAICINPhysicians Science & Nature Inc.05742cd5-ece2-4007-bdf0-46b76d23df742025-11-10WarningsExact identifier
ndc (product): 27495-014
074a8120-5d69-28ba-e063-6294a90a7e82cbf560f0-3bc3-51df-e053-2a95a90ab2982023-10-09WarningsExact identifier
spl set id: cbf560f0-3bc3-51df-e053-2a95a90ab298

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.