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NDC 49035-0295-10 Medicated Body 3; 20 mg/2g; mg/2g Details

Medicated Body 3; 20 mg/2g; mg/2g

Medicated Body is a TOPICAL POWDER in the HUMAN OTC DRUG category. It is labeled and distributed by Walmart Stores Inc. The primary component is MENTHOL; ZINC OXIDE.

Product Information

NDC	49035-0295
Product ID	49035-295_3af6617c-2131-49d5-8c3d-99d27cd3c253
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	Medicated Body
Proprietary Name Suffix	Powder
Non-Proprietary Name	MENTHOL, ZINC OXIDE
Product Type	HUMAN OTC DRUG
Dosage Form	POWDER
Route	TOPICAL
Active Ingredient Strength	3; 20
Active Ingredient Units	mg/2g; mg/2g
Substance Name	MENTHOL; ZINC OXIDE
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 49035-0295-10 (49035029510)

Pricing Information	N/A
NDC Package Code	49035-295-10
Billing NDC	49035029510
Package	283 g in 1 BOTTLE (49035-295-10)
Marketing Start Date	2009-09-01
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 206cd4f9-5829-41aa-8187-16728bcabfd7 Details

Drug FactsActive Ingredients

Menthol 0.15 %

Zinc Oxide 1.0%

Purpose

External Analgesic

Skin Protectant

Uses

for the temporary relief of the pain and itch associated with

minor cuts
scrapes
sunburn
insect bites
prickly heat
rashes
minor burns
minor skin irritations
dries the oozing of poison ivy, oak and sumac.

Keep out of reach of children

Keep out of reach of children. In case of accidential ingestion, get medical help or contact a Poison Control Center right away.

Warnings

For external use only

When usin this product

Avoid contact with eyes. Not for genital area.

Stop use and ask a doctor if

condition worsens
symptoms do not get better within 7 days or clear up and occur again within a few days

Directions

adults and children 2 years and older, apply freely up to 3 or 4 times daily
under 2 years: ask a doctor before using
for best results, dry skin thoroughly before use

Inactive Ingredients

Talc, Acacia, Eucalyputus Oil, Menthyl Salicylate, Salicylic Acid, Thymol, Zinc Stearate

equate Medicated Body Powder product label

NDC 49035-295-10

equate™

Compare to GoldBond® Medicated Body Powder Active Ingredients

Medicated Body Powder

4 X Relief

Relieves Itcing
Cools Skin
Absorbs Moisture
Helps Protect skin

Menthol 0.15%

NET WT 10 OZ (283g)

Medicated Body Powder

Satisfaction guarenteed- or we'll replace it or give you your money back.

For questions or comments or to report an undesired reaction or side effect, please call 1-888-287-1915

DISTRIBUTED BY:

Wal-Mart Stores, Inc.,

Bentonville, AR 72716

PRODUCT OF IINDIA

*This product is not manufactured or distributed by Chattem, Inc., owner of the registered trademark Gold Bond® Medicated body Powder.

DNH/C-92

INGREDIENTS AND APPEARANCE

MEDICATED BODY POWDER

menthol, zinc oxide powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:49035-295
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	3 mg in 2 g
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	20 mg in 2 g

Ingredient Name	Strength
Inactive Ingredients
TALC (UNII: 7SEV7J4R1U)
ACACIA (UNII: 5C5403N26O)
EUCALYPTUS OIL (UNII: 2R04ONI662)
MENTHYL SALICYLATE, (+/-)- (UNII: 43XOA705ZD)
SALICYLIC ACID (UNII: O414PZ4LPZ)
THYMOL (UNII: 3J50XA376E)
ZINC STEARATE (UNII: H92E6QA4FV)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:49035-295-10	283 g in 1 BOTTLE; Type 0: Not a Combination Product	09/01/2009

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part348	09/01/2009

Labeler - Walmart Stores Inc (051957769)

Revised: 12/2016

Document Id: 3af6617c-2131-49d5-8c3d-99d27cd3c253

Set id: 206cd4f9-5829-41aa-8187-16728bcabfd7

Version: 1

Effective Time: 20161218