Product NDC: | 0573-1935 |
Proprietary Name: | CHAPSTICK OVERNIGHT |
Non Proprietary Name: | dimethicone |
Active Ingredient(s): | 20 mg/g & nbsp; dimethicone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0573-1935 |
Labeler Name: | Pfizer Consumer Healthcare |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part347 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20040101 |
Package NDC: | 0573-1935-12 |
Package Description: | 1 TUBE in 1 BLISTER PACK (0573-1935-12) > 7 g in 1 TUBE |
NDC Code | 0573-1935-12 |
Proprietary Name | CHAPSTICK OVERNIGHT |
Package Description | 1 TUBE in 1 BLISTER PACK (0573-1935-12) > 7 g in 1 TUBE |
Product NDC | 0573-1935 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | dimethicone |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20040101 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Pfizer Consumer Healthcare |
Substance Name | DIMETHICONE |
Strength Number | 20 |
Strength Unit | mg/g |
Pharmaceutical Classes |