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ULTRA CORRECTION
ULTRA CORRECTION - 68745-1132-2 - (ANTI-WRINKLE DAY FLUID)
Drug Information of ULTRA CORRECTION
| Product NDC: | 68745-1132 |
| Proprietary Name: | ULTRA CORRECTION |
| Non Proprietary Name: | ANTI-WRINKLE DAY FLUID |
| Active Ingredient(s): | 1.5; 3.75 mL/50mL; mL/50mL & nbsp; ANTI-WRINKLE DAY FLUID |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | EMULSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ULTRA CORRECTION
| Product NDC: | 68745-1132 |
| Labeler Name: | CHANEL PARFUMS BEAUTE |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20090101 |
Package Information of ULTRA CORRECTION
| Package NDC: | 68745-1132-2 |
| Package Description: | 1 BOTTLE, PUMP in 1 CARTON (68745-1132-2) > 50 mL in 1 BOTTLE, PUMP (68745-1132-1) |
NDC Information of ULTRA CORRECTION
| NDC Code | 68745-1132-2 |
| Proprietary Name | ULTRA CORRECTION |
| Package Description | 1 BOTTLE, PUMP in 1 CARTON (68745-1132-2) > 50 mL in 1 BOTTLE, PUMP (68745-1132-1) |
| Product NDC | 68745-1132 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ANTI-WRINKLE DAY FLUID |
| Dosage Form Name | EMULSION |
| Route Name | TOPICAL |
| Start Marketing Date | 20090101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | CHANEL PARFUMS BEAUTE |
| Substance Name | AVOBENZONE; OCTINOXATE |
| Strength Number | 1.5; 3.75 |
| Strength Unit | mL/50mL; mL/50mL |
| Pharmaceutical Classes |
