Product NDC: | 68828-053 |
Proprietary Name: | JAFRA DAILY |
Non Proprietary Name: | ALUMINUM CHLOROHYDRATE |
Active Ingredient(s): | 12.3 g/100g & nbsp; ALUMINUM CHLOROHYDRATE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68828-053 |
Labeler Name: | JAFRA COSMETICS INTERNATIONAL |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part350 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120424 |
Package NDC: | 68828-053-52 |
Package Description: | 1 BOTTLE in 1 BOX (68828-053-52) > 60 g in 1 BOTTLE (68828-053-32) |
NDC Code | 68828-053-52 |
Proprietary Name | JAFRA DAILY |
Package Description | 1 BOTTLE in 1 BOX (68828-053-52) > 60 g in 1 BOTTLE (68828-053-32) |
Product NDC | 68828-053 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ALUMINUM CHLOROHYDRATE |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20120424 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | JAFRA COSMETICS INTERNATIONAL |
Substance Name | ALUMINUM CHLOROHYDRATE |
Strength Number | 12.3 |
Strength Unit | g/100g |
Pharmaceutical Classes |