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NDC 79903-0039-60 Equate Pain Relief Patch Camphor/Menthol/Salicylate 3.1; 6; 10 g/100g; g/100g; g/100g Details

Equate Pain Relief Patch Camphor/Menthol/Salicylate 3.1; 6; 10 g/100g; g/100g; g/100g

Equate Pain Relief Patch Camphor/Menthol/Salicylate is a PERCUTANEOUS; TOPICAL; TRANSDERMAL PATCH in the HUMAN OTC DRUG category. It is labeled and distributed by Walmart Stores Inc. The primary component is CAMPHOR (SYNTHETIC); MENTHOL; METHYL SALICYLATE.

Product Information

NDC	79903-0039
Product ID	79903-039_bd95a7b5-2ce6-9499-e053-2a95a90a7332
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Equate Pain Relief Patch Camphor/Menthol/Salicylate
Proprietary Name Suffix	n/a
Non-Proprietary Name	Camphor, Menthol, Methyl salicylate
Product Type	HUMAN OTC DRUG
Dosage Form	PATCH
Route	PERCUTANEOUS; TOPICAL; TRANSDERMAL
Active Ingredient Strength	3.1; 6; 10
Active Ingredient Units	g/100g; g/100g; g/100g
Substance Name	CAMPHOR (SYNTHETIC); MENTHOL; METHYL SALICYLATE
Labeler Name	Walmart Stores Inc
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH NOT FINAL
Application Number	part348
Listing Certified Through	2024-12-31

Package

Package Images

NDC 79903-0039-60 (79903003960)

Pricing Information	N/A
NDC Package Code	79903-039-60
Billing NDC	79903003960
Package	60 POUCH in 1 BOX (79903-039-60) / 6 g in 1 POUCH
Marketing Start Date	2021-01-01
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL b869848c-21e2-5ca2-e053-2995a90a86f2 Details

Active ingredients

Camphor 3.1%

Menthol 6.0%

Methyl salicylate 10.0%

Purpose

Topical analgesic

Uses

For temporary relief of minor aches and pains of muscles and joints associated with:

arthritis
simple backache
muscle strains
muscle sprains and bruises

Warnings

For external use only

Allergy alert:

If prone to allergic reaction from aspirin or salicylates, consult a doctor before use.

Do not use

on wounds or damaged skin
with a heating pad
if you are allergic to any ingredients of this product
Do not use otherwise than as directed

When using this product

use only as directed
avoid contact with the eyes, mucous membranes, or rashes
do not bandage tightly
Do not use at the same time as other topical analgesics
Dispose of used patch away from children and pets. Used patches still contain the drug product that can produce serious adverse effects if a child or pet chews or ingests this patch.

Stop use and ask a doctor if

rash, itching, or excessive skin irritation develops
conditions worsen
symptoms last for more than 7 days or clear up and occur again within a few days

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

Adults and children 12 years of age and over:

clean and dry affected area
remove patch from film
apply to affected area not more than 3 to 4 times daily
Do not use for more than 8 hours.
Discard patch after single use. Reseal pouch after opening.

Children under 12 years of age: consult a doctor

Other information

Store in a clean, dry place outside of direct sunlight. Protect for excessive moisture.

Inactive ingredients

hydrogenated poly, pentaerythrityl tetra-di-t-butyl hydroxyhydrocinnamate, petroleum, styrene/isoprene copolymer.

Equate Pain Relief Patch Camphor/Menthol/Salicylate

INGREDIENTS AND APPEARANCE

EQUATE PAIN RELIEF PATCH CAMPHOR/MENTHOL/SALICYLATE

camphor, menthol, methyl salicylate patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:79903-039
Route of Administration	TOPICAL, PERCUTANEOUS, TRANSDERMAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	3.1 g in 100 g
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	6 g in 100 g
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	10 g in 100 g

Ingredient Name	Strength
Inactive Ingredients
LIQUID PETROLEUM (UNII: 6ZAE7X688J)
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
STYRENE/ACRYLAMIDE COPOLYMER (MW 500000) (UNII: 5Z4DPO246A)
HYDROGENATED POLYDECENE TYPE I (UNII: U333RI6EB7)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:79903-039-60	60 in 1 BOX	01/01/2021
1		6 g in 1 POUCH; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part348	01/01/2021

Labeler - Walmart Stores Inc (051957769)

Name	Address	ID/FEI	Business Operations
Establishment
Foshan Aqua Gel Biotech Co., Ltd.,		529128763	manufacture(79903-039)

Revised: 3/2021

Document Id: bd95a7b5-2ce6-9499-e053-2a95a90a7332

Set id: b869848c-21e2-5ca2-e053-2995a90a86f2

Version: 4

Effective Time: 20210315