Product NDC: | 76209-123 |
Proprietary Name: | Cellular Laboratories De-Aging Sunscreen Broad Spectrum SPF 50 Plus |
Non Proprietary Name: | HOMOSALATE, OCTISALATE, AVOBENZONE, OCTOCRYLENE |
Active Ingredient(s): | 30; 100; 50; 26 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; HOMOSALATE, OCTISALATE, AVOBENZONE, OCTOCRYLENE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 76209-123 |
Labeler Name: | Market America |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110503 |
Package NDC: | 76209-123-01 |
Package Description: | 1 BOTTLE in 1 CARTON (76209-123-01) > 100 mL in 1 BOTTLE |
NDC Code | 76209-123-01 |
Proprietary Name | Cellular Laboratories De-Aging Sunscreen Broad Spectrum SPF 50 Plus |
Package Description | 1 BOTTLE in 1 CARTON (76209-123-01) > 100 mL in 1 BOTTLE |
Product NDC | 76209-123 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | HOMOSALATE, OCTISALATE, AVOBENZONE, OCTOCRYLENE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20110503 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Market America |
Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE |
Strength Number | 30; 100; 50; 26 |
Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
Pharmaceutical Classes |