PURE DRY- aluminum chlorohydrate liquid

Drug Labeling and Warnings

Drug Details [pdf]

WARNINGS

For external use only.
Do not use on broken skin.
Ask a doctor before use if you have kidney disease.
Stop use if rash or irritation occurs.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

PURPOSE

Antiperspirant, apply to underarms only

ACTIVE INGREDIENT

Aluminum Chlorohydrate 15% (9g/60mL)

INACTIVE INGREDIENT

Purified Water, Glycerin, Hydroxyethylcellulose, Phenoxyethanol, Ethylhexylglycerin, Allantoin, Aloe Barbadensis Leaf Juice Powder

INDICATIONS & USAGE

Reduces underarm wetness.

DOSAGE & ADMINISTRATION

Apply to underarms only.
Apply at bedtime to clean, fully dry underarms.
Apply sparingly — only a few strokes under each arm.
Do not apply immediately after shaving or on irritated skin.
For sensitive skin: start 2–3 nights per week, then increase as needed.
Let dry before dressing.

DRY GRIP PDP

INGREDIENTS AND APPEARANCE

PURE DRY 
aluminum chlorohydrate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85751-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M)	ALUMINUM CHLOROHYDRATE	15 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROXYETHYLCELLULOSE (UNII: T4V6TWG28D)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
ALLANTOIN (UNII: 344S277G0Z)
ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85751-003-02	1 in 1 BOX	04/22/2026
1	NDC: 85751-003-01	60 g in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M019	04/22/2026

Labeler - Chongqing Alefa Technology Co., Ltd. (409317595)

Establishment
Name	Address	ID/FEI	Business Operations
Chongqing Alefa Technology Co., Ltd.		409317595	manufacture(85751-003) , label(85751-003) , pack(85751-003)