| 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 |