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 |