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DAYWEAR
DAYWEAR - 11559-023-01 - (AVOBENZONE, OCTISALATE, and OCTOCRYLENE)
Drug Information of DAYWEAR
| Product NDC: | 11559-023 |
| Proprietary Name: | DAYWEAR |
| Non Proprietary Name: | AVOBENZONE, OCTISALATE, and OCTOCRYLENE |
| Active Ingredient(s): | .0303; .0505; .02727 g/mL; g/mL; g/mL & nbsp; AVOBENZONE, OCTISALATE, and OCTOCRYLENE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DAYWEAR
| Product NDC: | 11559-023 |
| Labeler Name: | ESTEE LAUDER INC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120101 |
Package Information of DAYWEAR
| Package NDC: | 11559-023-01 |
| Package Description: | 1 JAR in 1 CARTON (11559-023-01) > 50 mL in 1 JAR |
NDC Information of DAYWEAR
| NDC Code | 11559-023-01 |
| Proprietary Name | DAYWEAR |
| Package Description | 1 JAR in 1 CARTON (11559-023-01) > 50 mL in 1 JAR |
| Product NDC | 11559-023 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | AVOBENZONE, OCTISALATE, and OCTOCRYLENE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | ESTEE LAUDER INC |
| Substance Name | AVOBENZONE; OCTISALATE; OCTOCRYLENE |
| Strength Number | .0303; .0505; .02727 |
| Strength Unit | g/mL; g/mL; g/mL |
| Pharmaceutical Classes |
