| Product NDC: | 0573-1940 |
| Proprietary Name: | CHAPSTICK ULTRA SPF 30 |
| Non Proprietary Name: | OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE, PETROLATUM |
| Active Ingredient(s): | 75; 50; 70; 50; 300 mg/g; mg/g; mg/g; mg/g; mg/g & nbsp; OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE, PETROLATUM |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | STICK |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0573-1940 |
| Labeler Name: | Pfizer Consumer Healthcare |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20040130 |
| Package NDC: | 0573-1940-50 |
| Package Description: | 4 g in 1 CYLINDER (0573-1940-50) |
| NDC Code | 0573-1940-50 |
| Proprietary Name | CHAPSTICK ULTRA SPF 30 |
| Package Description | 4 g in 1 CYLINDER (0573-1940-50) |
| Product NDC | 0573-1940 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE, PETROLATUM |
| Dosage Form Name | STICK |
| Route Name | TOPICAL |
| Start Marketing Date | 20040130 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Pfizer Consumer Healthcare |
| Substance Name | OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE; PETROLATUM |
| Strength Number | 75; 50; 70; 50; 300 |
| Strength Unit | mg/g; mg/g; mg/g; mg/g; mg/g |
| Pharmaceutical Classes |