MEDICATED BODY- menthol, zinc oxide powder

Medicated Body by

Drug Labeling and Warnings

Medicated Body by is a Otc medication manufactured, distributed, or labeled by McKesson, Vi-Jon, M+K Packaging. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients
Menthol 0.15%
Zinc oxide 1.0%

Purpose
External analgesic
Skin protectant

INDICATIONS & USAGE

Uses for temporary relief of pain and itching due to:
minor cuts      sunburn           insect bites
poison ivy       poison oak      poison sumac
scrapes            minor burns    minor skin irritations
dries the oozing and weeping of:
poison ivy       poison oak      poison sumac

WARNINGS

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

DOSAGE & ADMINISTRATION

Directions
adults and children 2 years 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 INGREDIENT

Inactive ingredients talc, acacia, eucalyptol, methyl salicylate, salicylic acid, thymol, zinc stearate,

SPL UNCLASSIFIED SECTION

This product is not manufactured or distributed by Chattem, Inc., distributor of Gold Bond Medicated Body Powder.
This product is sold by weight, not volume.  Some settling may occur during handling and shippint

ADVERSE REACTIONS

Another Quality Product
Distributed By McKesson
One Post Street
San Francisco, CA 94104
Money Back Guarantee
Please visit us at
www.sunmarkbrand.com

PRINCIPAL DISPLAY PANEL

Sunmark
Compare to
Gold Bond
Medicated
Body
Powder
Skin Protectant
External Analgesic
Cooling
Absorbing
Itch Relieving
NET WT 10 OZ (283 g)

INGREDIENTS AND APPEARANCE

MEDICATED BODY 
menthol, zinc oxide powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49348-834
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	0.15 g  in 100 kg
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	1.0 g  in 100 kg

Inactive Ingredients
Ingredient Name	Strength
TALC (UNII: 7SEV7J4R1U)
ACACIA (UNII: 5C5403N26O)
EUCALYPTOL (UNII: RV6J6604TK)
METHYL SALICYLATE (UNII: LAV5U5022Y)
SALICYLIC ACID (UNII: O414PZ4LPZ)
THYMOL (UNII: 3J50XA376E)
ZINC STEARATE (UNII: H92E6QA4FV)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49348-834-92	.283 kg in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	06/18/1994

Labeler - McKesson (177667227)

Registrant - Vi-Jon (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
M+K Packaging		047022405	manufacture