DEODORANTANTIPERSPIRANTSPRAY- aluminum chlorohydrate liquid

DEODORANTANTIPERSPIRANTSPRAY by

Drug Labeling and Warnings

DEODORANTANTIPERSPIRANTSPRAY by is a Otc medication manufactured, distributed, or labeled by Shengnan (Guangzhou) Cosmetics Co., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

WARNINGS

Please keep out of reach of children.

PURPOSE

Reduces sweat production and keeps skin dry. While inhibiting sweat, it also prevents odor, ensuring a fresh body scent.

STOP USE

Discontinue use if skin shows abnormalreactions.A patch test on a small areaof skin is recommended before full use.

ACTIVE INGREDIENT

Aluminum Chlorohydrate

WHEN USING

Please keep your skin dry before use to ensure the best results fromthe product.

INACTIVE INGREDIENT

Butylene Glycol
Propylene Glycol
Alcohol
Water
Fragrance
Algin
Agar
Titanium Dioxide
Pentylene Glycol
Polyoxyethylene Cetyl Stearyl Diether
Stearic Acid
C12-16 Alcohols
Phenoxyethanol
Menthol
Salvia Miltiorrhiza Root Extract
Eugenia Caryophyllus (Clove) Bud Extract
Angelica Polymorpha Sinensis Root Extract
Centella Asiatica Extract
Glycyrrhiza Uralensis (Licorice) Root Extract
Jojoba Esters
CI 26100

DOSAGE & ADMINISTRATION

Apply 2 times a day

INDICATIONS & USAGE

Hold the bottle about 15 cm away fromthe underarm and spray evenly ontoclean, dry skin.

KEEP OUT OF REACH OF CHILDREN

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DEODORANTANTIPERSPIRANTSPRAY 
aluminum chlorohydrate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84019-022
Route of Administration	CUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M)	ALUMINUM CHLOROHYDRATE	100 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
WATER (UNII: 059QF0KO0R)
STEARIC ACID (UNII: 4ELV7Z65AP)
ALGIN (UNII: C269C4G2ZQ)
AGAR (UNII: 89T13OHQ2B)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84019-022-01	80 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/28/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	12/28/2024

Labeler - Shengnan (Guangzhou) Cosmetics Co., LTD (541200425)

Establishment
Name	Address	ID/FEI	Business Operations
Shengnan (Guangzhou) Cosmetics Co., LTD		541200425	manufacture(84019-022)