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EGF Premium Whitening Skin
EGF Premium Whitening Skin - 55133-050-01 - (Allantoin)
Drug Information of EGF Premium Whitening Skin
| Product NDC: | 55133-050 |
| Proprietary Name: | EGF Premium Whitening Skin |
| Non Proprietary Name: | Allantoin |
| Active Ingredient(s): | .75 mg/150mL & nbsp; Allantoin |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of EGF Premium Whitening Skin
| Product NDC: | 55133-050 |
| Labeler Name: | HANBANGMEIN COSMETICS |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121001 |
Package Information of EGF Premium Whitening Skin
| Package NDC: | 55133-050-01 |
| Package Description: | 150 mL in 1 CARTON (55133-050-01) |
NDC Information of EGF Premium Whitening Skin
| NDC Code | 55133-050-01 |
| Proprietary Name | EGF Premium Whitening Skin |
| Package Description | 150 mL in 1 CARTON (55133-050-01) |
| Product NDC | 55133-050 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Allantoin |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20121001 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | HANBANGMEIN COSMETICS |
| Substance Name | ALLANTOIN |
| Strength Number | .75 |
| Strength Unit | mg/150mL |
| Pharmaceutical Classes |
