JAFRA DAILY ANTIPERSPIRANT DEODORANT ROLL-ON- aluminum chlorohydrate liquid

Jafra Daily Antiperspirant Deodorant Roll-on by

Drug Labeling and Warnings

Jafra Daily Antiperspirant Deodorant Roll-on by is a Otc medication manufactured, distributed, or labeled by Jafra Cosmetics International, Distribuidora Comercial Jafra, S.A. de C.V.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient(s)

Aluminum Chlorohydrate 12.3% 

Purpose

Antiperspirant

Uses

Reduces underarm wetness

Warnings

For external use only
Do not useon broken skin
Stop useif rash or irritation occurs
Ask a doctorbefore use if you have kidney disease

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Apply to underarms only

INACTIVE INGREDIENT

Inactive Ingredients
Water/Aqua, PEG-40 Stearate, PEG-25 Propylene Glycol Stearate, Stearic Acid, Sorbitan Sesquioleate, Cetyl Alcohol, Magnesium Aluminum Silicate, Fragrance/Parfum, DMDM Hydantoin, Iodopropynyl Butylcarbamate

Product label

INGREDIENTS AND APPEARANCE

JAFRA DAILY ANTIPERSPIRANT DEODORANT ROLL-ON 
aluminum chlorohydrate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68828-702
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M)	ALUMINUM CHLOROHYDRATE	12.3 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PEG-40 STEARATE (UNII: ECU18C66Q7)
PEG-25 PROPYLENE GLYCOL STEARATE (UNII: X21KPH4633)
STEARIC ACID (UNII: 4ELV7Z65AP)
SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
DMDM HYDANTOIN (UNII: BYR0546TOW)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
CETYL ALCOHOL (UNII: 936JST6JCN)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68828-702-02	1 in 1 CARTON	12/31/2021
1	NDC: 68828-702-01	60 mL in 1 BOTTLE, WITH APPLICATOR; 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	12/31/2021

Labeler - Jafra Cosmetics International (041676479)

Registrant - Jafra Cosmetics International (041676479)

Establishment
Name	Address	ID/FEI	Business Operations
Distribuidora Comercial Jafra, S.A. de C.V.		951612777	manufacture(68828-702)