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CHAP-ET
CHAP-ET - 0135-0495-01 - (white petrolatum)
Drug Information of CHAP-ET
| Product NDC: | 0135-0495 |
| Proprietary Name: | CHAP-ET |
| Non Proprietary Name: | white petrolatum |
| Active Ingredient(s): | 619.3 mg/g & nbsp; white petrolatum |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIPSTICK |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CHAP-ET
| Product NDC: | 0135-0495 |
| Labeler Name: | GlaxoSmithKline Consumer Healthcare LP |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100920 |
Package Information of CHAP-ET
| Package NDC: | 0135-0495-01 |
| Package Description: | 4.5 g in 1 TUBE (0135-0495-01) |
NDC Information of CHAP-ET
| NDC Code | 0135-0495-01 |
| Proprietary Name | CHAP-ET |
| Package Description | 4.5 g in 1 TUBE (0135-0495-01) |
| Product NDC | 0135-0495 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | white petrolatum |
| Dosage Form Name | LIPSTICK |
| Route Name | TOPICAL |
| Start Marketing Date | 20100920 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | GlaxoSmithKline Consumer Healthcare LP |
| Substance Name | PETROLATUM |
| Strength Number | 619.3 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
