Product NDC: | 44924-112 |
Proprietary Name: | BABOR Stop Cellulite |
Non Proprietary Name: | Panthenol |
Active Ingredient(s): | .075 mL/10mL & nbsp; Panthenol |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 44924-112 |
Labeler Name: | Babor Cosmetics America, Corp |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20100410 |
Package NDC: | 44924-112-02 |
Package Description: | 14 AMPULE in 1 CARTON (44924-112-02) > 10 mL in 1 AMPULE (44924-112-01) |
NDC Code | 44924-112-02 |
Proprietary Name | BABOR Stop Cellulite |
Package Description | 14 AMPULE in 1 CARTON (44924-112-02) > 10 mL in 1 AMPULE (44924-112-01) |
Product NDC | 44924-112 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Panthenol |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20100410 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Babor Cosmetics America, Corp |
Substance Name | PANTHENOL |
Strength Number | .075 |
Strength Unit | mL/10mL |
Pharmaceutical Classes |