Product NDC: | 42248-121 |
Proprietary Name: | Sun Care |
Non Proprietary Name: | OCTINOXATE AVOBENZONE ZINC OXIDE OCTOCRYLENE |
Active Ingredient(s): | 1.8; 4.5; 4.5; 14.4 mL/60mL; mL/60mL; mL/60mL; mL/60mL & nbsp; OCTINOXATE AVOBENZONE ZINC OXIDE OCTOCRYLENE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | EMULSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 42248-121 |
Labeler Name: | Zenith Medicosm SL |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110815 |
Package NDC: | 42248-121-01 |
Package Description: | 60 mL in 1 TUBE (42248-121-01) |
NDC Code | 42248-121-01 |
Proprietary Name | Sun Care |
Package Description | 60 mL in 1 TUBE (42248-121-01) |
Product NDC | 42248-121 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE AVOBENZONE ZINC OXIDE OCTOCRYLENE |
Dosage Form Name | EMULSION |
Route Name | TOPICAL |
Start Marketing Date | 20110815 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Zenith Medicosm SL |
Substance Name | AVOBENZONE; OCTINOXATE; OCTOCRYLENE; ZINC OXIDE |
Strength Number | 1.8; 4.5; 4.5; 14.4 |
Strength Unit | mL/60mL; mL/60mL; mL/60mL; mL/60mL |
Pharmaceutical Classes |