BODY- menthol powder
Wal-Mart Stores, Inc

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Equate 379.001/379AB

Active ingredient

Menthol 0.15%

Purpose

External analgesic

Uses

for temporary relief of pain and itching associated with:

minor cuts
sunburn
insect bites
poison ivy
poison oak
poison sumac
scrapes
minor burns
minor skin irritations

warnings

For external use only

When using this product

avoid contact with the eyes

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

keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

adults and children 2 year of age and older - apply to affected area not more than 3 to 4 times daily
children under 2 years of age - do not use, consult a doctor
for best results dry skin thoroughly before applying

Inactive ingredients

Zea mays (corn) starch, sodium bicarbonate, tricalcium phosphate, zinc oxide, acacia seyal gum, eucalyptol, methyl salicylate, salicylic acid, thymol, zinc stearate

Questions

Call 1-888-287-1915

Questions

Call 1-888-287-1915

Satisfaction guaranteed

Satisfaction Guaranteed-For questions or comments please call 1-888-287-1915

disclaimers

This product is not manufactured or distributed by chattem, distrobutor of Gold Bond Medicated Body powder.

This product is sold by weight, not by volume. Some settling may occur during handling and shipping.

Adverse reactions

Distributed by: Wal-Mart Stores, Inc., Bentonville, AR 72716

379.001/AB

principal display panel

equate

Compare to

Gold Bond

Medicated

Body

Powder

Medicated

Body Powder

PAIN RELIEVING POWDER

TRIPLE BENEFITS

Cooling
Abosrbent
Itch-relieving

Menthol 0.15%

NET WT 10 OZ (283 g)

image description

BODY
menthol powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:49035-071
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	1.5 mg in 1 g

Ingredient Name	Strength
Inactive Ingredients
STARCH, CORN (UNII: O8232NY3SJ)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
TRICALCIUM PHOSPHATE (UNII: K4C08XP666)
ZINC OXIDE (UNII: SOI2LOH54Z)
GUM TALHA (UNII: H18F76G097)
EUCALYPTOL (UNII: RV6J6604TK)
METHYL SALICYLATE (UNII: LAV5U5022Y)
SALICYLIC ACID (UNII: O414PZ4LPZ)
THYMOL (UNII: 3J50XA376E)
ZINC STEARATE (UNII: H92E6QA4FV)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:49035-071-38	283 g in 1 BOTTLE; Type 0: Not a Combination Product	01/10/2012	04/20/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part348	01/10/2012	04/20/2021

Labeler - Wal-Mart Stores, Inc (051957769)

Registrant - Vi-Jon, LLC (790752542)

Name	Address	ID/FEI	Business Operations
Establishment
MK Packaging		047022405	manufacture(49035-071)

Revised: 4/2021

Document Id: a1f95658-c3ff-41fc-b1ac-3d98d2d57f59

Set id: 8e14c6df-00e2-48e9-9a1c-c9149ea94fe4

Version: 7

Effective Time: 20210420

Wal-Mart Stores, Inc