NDC | 68828-053-32, 68828-053-52 |
Set ID | 4fa7e727-659a-45ea-b8d0-f9adb98c9f49 |
Category | HUMAN OTC DRUG LABEL |
Packager | JAFRA COSMETICS INTERNATIONAL |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART350 |
- ACTIVE INGREDIENT
- PURPOSE
- INACTIVE INGREDIENT
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- WARNINGS
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- PRINCIPAL DISPLAY PANEL
- ASK DOCTOR
-
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)