| 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 |