| Product NDC: | 44924-100 |
| Proprietary Name: | Moderate Protection Sun SPF 15 |
| Non Proprietary Name: | Octocrylene |
| Active Ingredient(s): | 6; 15; 20; 4 mL/200mL; mL/200mL; mL/200mL; mL/200mL & nbsp; Octocrylene |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 44924-100 |
| Labeler Name: | Babor Cosmetics America, Corp |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100301 |
| Package NDC: | 44924-100-02 |
| Package Description: | 1 BOTTLE, SPRAY in 1 CARTON (44924-100-02) > 200 mL in 1 BOTTLE, SPRAY (44924-100-01) |
| NDC Code | 44924-100-02 |
| Proprietary Name | Moderate Protection Sun SPF 15 |
| Package Description | 1 BOTTLE, SPRAY in 1 CARTON (44924-100-02) > 200 mL in 1 BOTTLE, SPRAY (44924-100-01) |
| Product NDC | 44924-100 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octocrylene |
| Dosage Form Name | SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20100301 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Babor Cosmetics America, Corp |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTOCRYLENE; SULISOBENZONE |
| Strength Number | 6; 15; 20; 4 |
| Strength Unit | mL/200mL; mL/200mL; mL/200mL; mL/200mL |
| Pharmaceutical Classes |