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: | 0573-1940-24 |
Package Description: | 1 CYLINDER in 1 BLISTER PACK (0573-1940-24) > 4 g in 1 CYLINDER |
NDC Code | 0573-1940-24 |
Proprietary Name | CHAPSTICK ULTRA SPF 30 |
Package Description | 1 CYLINDER in 1 BLISTER PACK (0573-1940-24) > 4 g in 1 CYLINDER |
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 |