OTC Medication Information: JAFRA DAILY POWDER FRESH FOR WOMEN

JAFRA DAILY POWDER FRESH FOR WOMEN- aluminum chlorohydrate lotion
JAFRA COSMETICS INTERNATIONAL

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

ACTIVE INGREDIENT:
ALUMINUM CHLOROHYDRATE 12.3%

PURPOSE

ANTIPERSPIRANT

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.

USES

  • REDUCES UNDERARM WETNESS

DIRECTIONS

  • APPLY TO UNDERARMS ONLY

WARNINGS

  • DO NOT USE ON BROKEN SKIN.
  • STOP USE IF RASH OR IRRITATION OCCURS.

KEEP OUT OF REACH OF CHILDREN.

JAFRA


POWDER FRESH
FOR WOMEN
ANTIPERSPIRANT
DEODORANT ROLL-ON
60 G / NET WT 2 OZ
Powder Fresh A-P 2oz Primary
(click image for full-size original)
Powder Fresh A-P 2oz Secondary
(click image for full-size original)
  • ASK A DOCTOR BEFORE USE IF YOU HAVE KIDNEY DISEASE.
JAFRA DAILY POWDER FRESH FOR WOMEN
aluminum chlorohydrate lotion
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:68828-053
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALUMINUM CHLOROHYDRATE (ALUMINUM CATION) ALUMINUM CHLOROHYDRATE 12.3 g in 100 g
Inactive Ingredients
Ingredient Name Strength
WATER
PEG-40 STEARATE
PEG-25 PROPYLENE GLYCOL STEARATE
STEARIC ACID
SORBITAN SESQUIOLEATE
CETYL ALCOHOL
DMDM HYDANTOIN
MAGNESIUM ALUMINUM SILICATE
IODOPROPYNYL BUTYLCARBAMATE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:68828-053-52 1 BOTTLE (BOTTLE) in 1 BOX contains a BOTTLE (68828-053-32)
1 NDC:68828-053-32 60 g in 1 BOTTLE This package is contained within the BOX (68828-053-52)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part350 04/24/2012
Labeler — JAFRA COSMETICS INTERNATIONAL (041676479)

Revised: 05/2012 JAFRA COSMETICS INTERNATIONAL

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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