| Product NDC: | 44924-016 |
| Proprietary Name: | BABOR Collagen Booster |
| Non Proprietary Name: | Allantoin |
| Active Ingredient(s): | .004 mL/2mL & nbsp; Allantoin |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 44924-016 |
| Labeler Name: | Babor Cosmetics America, Corp. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20070501 |
| Package NDC: | 44924-016-02 |
| Package Description: | 7 AMPULE in 1 BOX (44924-016-02) > 2 mL in 1 AMPULE (44924-016-01) |
| NDC Code | 44924-016-02 |
| Proprietary Name | BABOR Collagen Booster |
| Package Description | 7 AMPULE in 1 BOX (44924-016-02) > 2 mL in 1 AMPULE (44924-016-01) |
| Product NDC | 44924-016 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Allantoin |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20070501 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Babor Cosmetics America, Corp. |
| Substance Name | ALLANTOIN |
| Strength Number | .004 |
| Strength Unit | mL/2mL |
| Pharmaceutical Classes |