Product NDC: | 51270-116 |
Proprietary Name: | Hasol Revitalizing Scalp Ampoule |
Non Proprietary Name: | ALLANTOIN |
Active Ingredient(s): | .1 g/10g & nbsp; ALLANTOIN |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51270-116 |
Labeler Name: | Ecomine Co Ltd |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part347 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20130701 |
Package NDC: | 51270-116-02 |
Package Description: | 12 BOTTLE in 1 BOX (51270-116-02) > 10 g in 1 BOTTLE (51270-116-01) |
NDC Code | 51270-116-02 |
Proprietary Name | Hasol Revitalizing Scalp Ampoule |
Package Description | 12 BOTTLE in 1 BOX (51270-116-02) > 10 g in 1 BOTTLE (51270-116-01) |
Product NDC | 51270-116 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ALLANTOIN |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20130701 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Ecomine Co Ltd |
Substance Name | ALLANTOIN |
Strength Number | .1 |
Strength Unit | g/10g |
Pharmaceutical Classes |