DERMFREE WHOLE BODY DEODORANT- aluminum chlorohydrate 9%whole body deodorant cream

DERMFREE Whole Body Deodorant by

Drug Labeling and Warnings

DERMFREE Whole Body Deodorant by is a Otc medication manufactured, distributed, or labeled by Jiangxi Hemei Pharmaceutical Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Aluminum chlorohydrate 9%

Purpose

Antiperspirant

Use

.Reduces underamm sweat
.24 hour effective protection

Warnings

For external use only

Do not use

on broken skin

When Using

Apply to underarms only

Stop Use

rash or irritation occurs

Ask Doctor

Ask a doctor before use ifyou have kidney disease

Keep Oot Of Reach Of Children

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

Directions

Apply to underarms only

Inactive ingredients

Cetyl alcohol,deionized water, glycerin, GLYCERYL MONOOLEATE,GLYCERYL MONOSTEARATE,GR-270773 PHOSPHOLIPID EMULSION, Silicone Oil, zinc phenolsulfonateetc

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DERMFREE WHOLE BODY DEODORANT 
aluminum chlorohydrate 9%whole body deodorant cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84010-015
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M)	ALUMINUM CHLOROHYDRATE	9 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
GLYCERYL MONOOLEATE (UNII: C4YAD5F5G6)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
CETYL ALCOHOL (UNII: 936JST6JCN)
WATER (UNII: 059QF0KO0R)
GR-270773 PHOSPHOLIPID EMULSION (UNII: D4B2F53PBH)
DIMETHICONE (UNII: 92RU3N3Y1O)
GLYCERIN (UNII: PDC6A3C0OX)
ZINC PHENOLSULFONATE (UNII: 4O71YT5YB5)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84010-015-01	85 g in 1 BOTTLE; Type 0: Not a Combination Product	04/30/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M019	04/30/2024

Labeler - Jiangxi Hemei Pharmaceutical Co., Ltd (724892056)

Establishment
Name	Address	ID/FEI	Business Operations
Jiangxi Hemei Pharmaceutical Co., Ltd		724892056	manufacture(84010-015)