Product NDC: | 58668-4531 |
Proprietary Name: | Clarins Sunscreen Care Radiant SPF 6 UVB/UVA |
Non Proprietary Name: | OCTINOXATE, AVOBENZONE |
Active Ingredient(s): | 3; 7.5 mL/100mL; mL/100mL & nbsp; OCTINOXATE, AVOBENZONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 58668-4531 |
Labeler Name: | Laboratoires Clarins S.A. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20101019 |
Package NDC: | 58668-4531-1 |
Package Description: | 1 BOTTLE in 1 PACKAGE (58668-4531-1) > 150 mL in 1 BOTTLE |
NDC Code | 58668-4531-1 |
Proprietary Name | Clarins Sunscreen Care Radiant SPF 6 UVB/UVA |
Package Description | 1 BOTTLE in 1 PACKAGE (58668-4531-1) > 150 mL in 1 BOTTLE |
Product NDC | 58668-4531 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE, AVOBENZONE |
Dosage Form Name | SPRAY |
Route Name | TOPICAL |
Start Marketing Date | 20101019 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Laboratoires Clarins S.A. |
Substance Name | AVOBENZONE; OCTINOXATE |
Strength Number | 3; 7.5 |
Strength Unit | mL/100mL; mL/100mL |
Pharmaceutical Classes |