DG Medicated Body Powder by Davion Inc

DG Medicated Body Powder by

Drug Labeling and Warnings

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

Drug Details [pdf]

DG MEDICATED BODY POWDER- menthol powder 
Davion Inc

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Active Ingredient

Menthol 0.15%

Purpose

External Analgesic

Uses

temporarily relives pain and itch associated with:

• Minor Cuts
• Sunburn
• Insect Bites
• Scrapes
• Minor Burns
• Minor Skin Irritation

Warning Section

• For external use only
• Avoid contact with eyes

Stop use and ask a doctor

If

• Conditions worsens
• symptoms persists for more than 7 days or clear up and occur again within a few days

Keep out of reach of children

In case of accidental ingestion get medical help or contact a Poison Control Centre right away

Directions

Remove seal beneath cap before first use. Do not use if the seal is broken or missing

• adults and children 2 years and older - apply freely up to 3 or 4 times daily
• childrens under 2 years - ask a doctor

For best results, dry skin thoroughly before applying.

Inactive Ingredients

Zea Mays (Corn) Starch, Zinc Oxide, Tricalcium Phosphate, Sodium Bicarbonate, Salicylic Acid, Zinc Stearate, Eucalyptus Oil, Peppermint Oil

Principal Display Panel

NDC: 42669-288-10

DG Body

Compare to the active ingredient of Gold Bond Medicated Body Powder

Medicated Body Poweder

• Cools
• Absorbs
• Relieves Itching

Talc-Free Made with Cornstarch

NET WT 10OZ (283 g)

DG MEDICATED BODY POWDER 
menthol powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 42669-288
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 1 g

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)	Â
SALICYLIC ACID (UNII: O414PZ4LPZ)	Â
ZINC STEARATE (UNII: H92E6QA4FV)	Â
STARCH, CORN (UNII: O8232NY3SJ)	Â
ZINC OXIDE (UNII: SOI2LOH54Z)	Â
EUCALYPTUS OIL (UNII: 2R04ONI662)	Â
PEPPERMINT OIL (UNII: AV092KU4JH)	Â
TRICALCIUM PHOSPHATE (UNII: K4C08XP666)	Â

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 42669-288-10	283 g in 1 BOTTLE; Type 0: Not a Combination Product	07/25/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	07/25/2023	12/22/2023

Labeler - Davion Inc (174542928)

Revised: 1/2024

Document Id: 0e24845f-a54d-5d02-e063-6394a90a4d6a

34390-5

Set id: 015460de-f0b8-ee59-e063-6394a90a5664

Version: 2

Effective Time: 20240104

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