Product NDC: | 76229-123 |
Proprietary Name: | Likewise Hand Moisturizer - Sun Protectant SPF 50 |
Non Proprietary Name: | OCTINOXATE, OCTISALATE, ZINC OXIDE |
Active Ingredient(s): | 7.5; 5; 11.16 mL/100mL; mL/100mL; mL/100mL & nbsp; OCTINOXATE, OCTISALATE, ZINC OXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 76229-123 |
Labeler Name: | Likewise Incorporated |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110620 |
Package NDC: | 76229-123-01 |
Package Description: | 1 BOTTLE in 1 PACKAGE (76229-123-01) > 85 mL in 1 BOTTLE |
NDC Code | 76229-123-01 |
Proprietary Name | Likewise Hand Moisturizer - Sun Protectant SPF 50 |
Package Description | 1 BOTTLE in 1 PACKAGE (76229-123-01) > 85 mL in 1 BOTTLE |
Product NDC | 76229-123 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE, OCTISALATE, ZINC OXIDE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20110620 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Likewise Incorporated |
Substance Name | OCTINOXATE; OCTISALATE; ZINC OXIDE |
Strength Number | 7.5; 5; 11.16 |
Strength Unit | mL/100mL; mL/100mL; mL/100mL |
Pharmaceutical Classes |