Jafra Daily Antiperspirant Rollon by Jafra Cosmetics International Inc / Distribuidora Comercial Jafra, S.A. de C.V.

Jafra Daily Antiperspirant Rollon by

Drug Labeling and Warnings

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

Drug Details [pdf]

JAFRA DAILY ANTIPERSPIRANT ROLLON- aluminum chlorohydrate liquid 
Jafra Cosmetics International Inc

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Active ingredient

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

Direction

Apply to underarms only

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

image description

JAFRA DAILY ANTIPERSPIRANT ROLLON 
aluminum chlorohydrate liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 68828-503
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE12.3 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
PEG-40 STEARATE (UNII: ECU18C66Q7)  
PEG-25 PROPYLENE GLYCOL STEARATE (UNII: X21KPH4633)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)  
DMDM HYDANTOIN (UNII: BYR0546TOW)  
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 68828-503-011 in 1 CARTON09/14/202211/30/2023
190 mL in 1 APPLICATOR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02009/14/202211/30/2023
Labeler - Jafra Cosmetics International Inc (041676479)
Establishment
NameAddressID/FEIBusiness Operations
Distribuidora Comercial Jafra, S.A. de C.V.951612777manufacture(68828-503)

Revised: 1/2024