| Product NDC: | 49527-035 |
| Proprietary Name: | CLINIQUE |
| Non Proprietary Name: | AVOBENZONE, OCTINOXATE, and OCTISALATE |
| Active Ingredient(s): | .0203; .076; .0507 g/mL; g/mL; g/mL & nbsp; AVOBENZONE, OCTINOXATE, and OCTISALATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 49527-035 |
| Labeler Name: | CLINIQUE LABORATORIES INC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100714 |
| Package NDC: | 49527-035-01 |
| Package Description: | 1 BOTTLE in 1 CARTON (49527-035-01) > 50 mL in 1 BOTTLE |
| NDC Code | 49527-035-01 |
| Proprietary Name | CLINIQUE |
| Package Description | 1 BOTTLE in 1 CARTON (49527-035-01) > 50 mL in 1 BOTTLE |
| Product NDC | 49527-035 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | AVOBENZONE, OCTINOXATE, and OCTISALATE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20100714 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | CLINIQUE LABORATORIES INC. |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE |
| Strength Number | .0203; .076; .0507 |
| Strength Unit | g/mL; g/mL; g/mL |
| Pharmaceutical Classes |