| Product NDC: | 44924-121 |
| Proprietary Name: | PURE SELECT Purifying Anti-Aging |
| Non Proprietary Name: | Allantoin |
| Active Ingredient(s): | .1 mL/50mL & nbsp; Allantoin |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 44924-121 |
| Labeler Name: | Babor Cosmetics America, Corp |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100615 |
| Package NDC: | 44924-121-02 |
| Package Description: | 1 BOTTLE, PUMP in 1 BOX (44924-121-02) > 50 mL in 1 BOTTLE, PUMP (44924-121-01) |
| NDC Code | 44924-121-02 |
| Proprietary Name | PURE SELECT Purifying Anti-Aging |
| Package Description | 1 BOTTLE, PUMP in 1 BOX (44924-121-02) > 50 mL in 1 BOTTLE, PUMP (44924-121-01) |
| Product NDC | 44924-121 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Allantoin |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20100615 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Babor Cosmetics America, Corp |
| Substance Name | ALLANTOIN |
| Strength Number | .1 |
| Strength Unit | mL/50mL |
| Pharmaceutical Classes |