| 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 |