Product NDC: | 76224-101 |
Proprietary Name: | SPF 15 |
Non Proprietary Name: | OCTINOXATE,OXYBENZONE |
Active Ingredient(s): | 7.5; 5 mL/100mL; mL/100mL & nbsp; OCTINOXATE,OXYBENZONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 76224-101 |
Labeler Name: | Whish Body Holdings Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110525 |
Package NDC: | 76224-101-02 |
Package Description: | 1 BOTTLE in 1 BOX (76224-101-02) > 150 mL in 1 BOTTLE (76224-101-01) |
NDC Code | 76224-101-02 |
Proprietary Name | SPF 15 |
Package Description | 1 BOTTLE in 1 BOX (76224-101-02) > 150 mL in 1 BOTTLE (76224-101-01) |
Product NDC | 76224-101 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE,OXYBENZONE |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20110525 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Whish Body Holdings Inc |
Substance Name | OCTINOXATE; OXYBENZONE |
Strength Number | 7.5; 5 |
Strength Unit | mL/100mL; mL/100mL |
Pharmaceutical Classes |