Label: JAFRA DAILY POWDER FRESH FOR WOMEN- aluminum chlorohydrate lotion
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Contains inactivated NDC Code(s)
NDC Code(s): 68828-053-32, 68828-053-52 - Packager: JAFRA COSMETICS INTERNATIONAL
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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.
Drug Label Information
Updated May 1, 2012
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- ACTIVE INGREDIENT
- PURPOSE
- INACTIVE INGREDIENT
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- WARNINGS
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- PRINCIPAL DISPLAY PANEL
- ASK DOCTOR
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INGREDIENTS AND APPEARANCE
JAFRA DAILY POWDER FRESH FOR WOMEN
aluminum chlorohydrate lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68828-053 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CATION - UNII:3XHB1D032B) ALUMINUM CHLOROHYDRATE 12.3 g in 100 g 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) CETYL ALCOHOL (UNII: 936JST6JCN) DMDM HYDANTOIN (UNII: BYR0546TOW) MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC) IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68828-053-52 1 in 1 BOX 1 NDC:68828-053-32 60 g in 1 BOTTLE 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)
