Product NDC: | 58668-4091 |
Proprietary Name: | CLARINS BROAD SPECTRUM SPF 30 - SUNSCREEN CARE |
Non Proprietary Name: | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE |
Active Ingredient(s): | 30; 100; 50; 27; 30 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL & nbsp; AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 58668-4091 |
Labeler Name: | Laboratoires Clarins S.A. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20130508 |
Package NDC: | 58668-4091-1 |
Package Description: | 1 BOTTLE in 1 CARTON (58668-4091-1) > 125 mL in 1 BOTTLE |
NDC Code | 58668-4091-1 |
Proprietary Name | CLARINS BROAD SPECTRUM SPF 30 - SUNSCREEN CARE |
Package Description | 1 BOTTLE in 1 CARTON (58668-4091-1) > 125 mL in 1 BOTTLE |
Product NDC | 58668-4091 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20130508 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Laboratoires Clarins S.A. |
Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
Strength Number | 30; 100; 50; 27; 30 |
Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL; mg/mL |
Pharmaceutical Classes |