Product NDC: | 42893-040 |
Proprietary Name: | CHANTECAILLE ULTRA SUN PROTECTION SPF 50 ANTI-GLYCATION PRIMER |
Non Proprietary Name: | OCTINOXATE, OCTISALATE, AVOBENZONE |
Active Ingredient(s): | 3; 7.5; 5 mL/100mL; mL/100mL; mL/100mL & nbsp; OCTINOXATE, OCTISALATE, AVOBENZONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 42893-040 |
Labeler Name: | Chantecaille Beaute Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120307 |
Package NDC: | 42893-040-00 |
Package Description: | 1 TUBE in 1 CARTON (42893-040-00) > 40 mL in 1 TUBE |
NDC Code | 42893-040-00 |
Proprietary Name | CHANTECAILLE ULTRA SUN PROTECTION SPF 50 ANTI-GLYCATION PRIMER |
Package Description | 1 TUBE in 1 CARTON (42893-040-00) > 40 mL in 1 TUBE |
Product NDC | 42893-040 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE, OCTISALATE, AVOBENZONE |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20120307 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Chantecaille Beaute Inc |
Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE |
Strength Number | 3; 7.5; 5 |
Strength Unit | mL/100mL; mL/100mL; mL/100mL |
Pharmaceutical Classes |