| 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 |