Perfect Purity Medicated Body Powder

Perfect Purity Medicated Body Powder by

Drug Labeling and Warnings

Perfect Purity Medicated Body Powder by is a Otc medication manufactured, distributed, or labeled by Davion, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PERFECT PURITY MEDICATED BODY POWDER- menthol and zinc oxide powder 
Davion, 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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Perfect Purity Medicated Body Powder

Active Ingredients

Menthol 0.15%
Zinc Oxide 1.0%

Purpose

Anti-itch
Skin Protectant

Uses

temporarily relieves pain and itch associated with:

• Minor Cuts
• Sunburn
• Insect Bites
• Scrapes
• Prickly Heat
• Minor Burns
• Rashes
• Minor Skin Irritations
• Dries the oozing of poison ivy, oak, and sumac.

Warning

For external use only.

• Avoid contact with eyes

Stop use and ask a doctor if

• condition worsens
• symptoms do not get better within 7 days

Keep Out of Reach of Children

In case of accidental ingestion, get medical help or contact a Poison Control Center right away.

Directions

• adults and children 2 years and older apply freely up to 3 or 4 times daily.
• children under 2 years ask a doctor.
• For best results, dry skin thoroughly before applying.

Inactive Ingredients

talc, eucalyptol, methyl salicylate, salicylic acid, thymol, zinc stearate.

Product Label

PERFECT PURITY MEDICATED BODY POWDER 
menthol and zinc oxide powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 42669-200
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 g
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
TALC (UNII: 7SEV7J4R1U)
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: 42669-200-01	283 g in 1 CONTAINER; Type 0: Not a Combination Product	12/05/2022	07/31/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	07/06/2010	07/31/2023

Labeler - Davion, Inc. (174542928)

Registrant - Davion, Inc. (174542928)

Establishment
Name	Address	ID/FEI	Business Operations
Davion, INc		079536689	manufacture(42669-200)

Revised: 7/2023

Document Id: 01ccfa74-aeba-d5ac-e063-6394a90a92fe

34390-5

Set id: 287f6300-6704-4a42-ba0b-70bf314df098

Version: 4

Effective Time: 20230731

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