Product NDC: | 10345-023 |
Proprietary Name: | Sun Verbena Protective Body Protection SPF 15 |
Non Proprietary Name: | OCTINOXATE, OCTISALATE, AVOBENZONE, OCTOCRYLENE |
Active Ingredient(s): | 23; 35; 50; 20 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; OCTINOXATE, OCTISALATE, AVOBENZONE, OCTOCRYLENE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10345-023 |
Labeler Name: | LABORATOIRES M&L |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110914 |
Package NDC: | 10345-023-01 |
Package Description: | 1 BOTTLE in 1 PACKAGE (10345-023-01) > 250 mL in 1 BOTTLE |
NDC Code | 10345-023-01 |
Proprietary Name | Sun Verbena Protective Body Protection SPF 15 |
Package Description | 1 BOTTLE in 1 PACKAGE (10345-023-01) > 250 mL in 1 BOTTLE |
Product NDC | 10345-023 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE, OCTISALATE, AVOBENZONE, OCTOCRYLENE |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20110914 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | LABORATOIRES M&L |
Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE; OCTOCRYLENE |
Strength Number | 23; 35; 50; 20 |
Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
Pharmaceutical Classes |