| Product NDC: | 31720-302 |
| Proprietary Name: | SEPHORA Sunscreen Body Mist Broad Spectrum SPF 30 |
| Non Proprietary Name: | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE |
| Active Ingredient(s): | 12; 60; 20; 8; 20 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL & nbsp; AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 31720-302 |
| Labeler Name: | S+ |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130228 |
| Package NDC: | 31720-302-13 |
| Package Description: | 1 BOTTLE, SPRAY in 1 PACKAGE (31720-302-13) > 150 mL in 1 BOTTLE, SPRAY |
| NDC Code | 31720-302-13 |
| Proprietary Name | SEPHORA Sunscreen Body Mist Broad Spectrum SPF 30 |
| Package Description | 1 BOTTLE, SPRAY in 1 PACKAGE (31720-302-13) > 150 mL in 1 BOTTLE, SPRAY |
| Product NDC | 31720-302 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20130228 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | S+ |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 12; 60; 20; 8; 20 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |