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CHAPSTICK ULTRA MOISTURE
CHAPSTICK ULTRA MOISTURE - 0573-1993-03 - (octinoxate, oxybenzone, petrolatum)
Drug Information of CHAPSTICK ULTRA MOISTURE
| Product NDC: | 0573-1993 |
| Proprietary Name: | CHAPSTICK ULTRA MOISTURE |
| Non Proprietary Name: | octinoxate, oxybenzone, petrolatum |
| Active Ingredient(s): | 75; 35; 330 mg/g; mg/g; mg/g & nbsp; octinoxate, oxybenzone, petrolatum |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CHAPSTICK ULTRA MOISTURE
| Product NDC: | 0573-1993 |
| Labeler Name: | Pfizer Consumer Healthcare |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20101209 |
Package Information of CHAPSTICK ULTRA MOISTURE
| Package NDC: | 0573-1993-03 |
| Package Description: | 1 TUBE in 1 BLISTER PACK (0573-1993-03) > 10 g in 1 TUBE |
NDC Information of CHAPSTICK ULTRA MOISTURE
| NDC Code | 0573-1993-03 |
| Proprietary Name | CHAPSTICK ULTRA MOISTURE |
| Package Description | 1 TUBE in 1 BLISTER PACK (0573-1993-03) > 10 g in 1 TUBE |
| Product NDC | 0573-1993 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | octinoxate, oxybenzone, petrolatum |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20101209 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Pfizer Consumer Healthcare |
| Substance Name | OCTINOXATE; OXYBENZONE; PETROLATUM |
| Strength Number | 75; 35; 330 |
| Strength Unit | mg/g; mg/g; mg/g |
| Pharmaceutical Classes |
