Product NDC: | 58668-4441 |
Proprietary Name: | Clarins Sunscreen Spray Oil-Free Progressive Tanning SPF 15 |
Non Proprietary Name: | HOMOSALATE, OCTINOXATE, OXYBENZONE, OCTISALATE, AVOBENZONE |
Active Ingredient(s): | 3; 8; 7.5; 5; 5 mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; HOMOSALATE, OCTINOXATE, OXYBENZONE, OCTISALATE, AVOBENZONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 58668-4441 |
Labeler Name: | Laboratoires Clarins S.A. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100805 |
Package NDC: | 58668-4441-1 |
Package Description: | 1 BOTTLE in 1 PACKAGE (58668-4441-1) > 150 mL in 1 BOTTLE |
NDC Code | 58668-4441-1 |
Proprietary Name | Clarins Sunscreen Spray Oil-Free Progressive Tanning SPF 15 |
Package Description | 1 BOTTLE in 1 PACKAGE (58668-4441-1) > 150 mL in 1 BOTTLE |
Product NDC | 58668-4441 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | HOMOSALATE, OCTINOXATE, OXYBENZONE, OCTISALATE, AVOBENZONE |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20100805 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Laboratoires Clarins S.A. |
Substance Name | AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OXYBENZONE |
Strength Number | 3; 8; 7.5; 5; 5 |
Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL |
Pharmaceutical Classes |