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DAYWEAR
DAYWEAR - 11559-008-01 - (OCTISALATE, AVOBENZONE)
Drug Information of DAYWEAR
| Product NDC: | 11559-008 |
| Proprietary Name: | DAYWEAR |
| Non Proprietary Name: | OCTISALATE, AVOBENZONE |
| Active Ingredient(s): | 3; 5 mL/100mL; mL/100mL & nbsp; OCTISALATE, AVOBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DAYWEAR
| Product NDC: | 11559-008 |
| Labeler Name: | ESTEE LAUDER INC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100901 |
Package Information of DAYWEAR
| Package NDC: | 11559-008-01 |
| Package Description: | 1 TUBE in 1 TUBE (11559-008-01) > 50 mL in 1 TUBE (11559-008-02) |
NDC Information of DAYWEAR
| NDC Code | 11559-008-01 |
| Proprietary Name | DAYWEAR |
| Package Description | 1 TUBE in 1 TUBE (11559-008-01) > 50 mL in 1 TUBE (11559-008-02) |
| Product NDC | 11559-008 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTISALATE, AVOBENZONE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20100901 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | ESTEE LAUDER INC |
| Substance Name | AVOBENZONE; OCTISALATE |
| Strength Number | 3; 5 |
| Strength Unit | mL/100mL; mL/100mL |
| Pharmaceutical Classes |
