| Product NDC: | 62191-007 |
| Proprietary Name: | Protective Foundation Sunscreen SPF 15 |
| Non Proprietary Name: | Sunscreen, AVOBENZONE, OCTINOXATE |
| Active Ingredient(s): | .02; .06 g/g; g/g & nbsp; Sunscreen, AVOBENZONE, OCTINOXATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | EMULSION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 62191-007 |
| Labeler Name: | Sunrider Manufacturing L.P. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20020301 |
| Package NDC: | 62191-007-02 |
| Package Description: | 30 g in 1 TUBE (62191-007-02) |
| NDC Code | 62191-007-02 |
| Proprietary Name | Protective Foundation Sunscreen SPF 15 |
| Package Description | 30 g in 1 TUBE (62191-007-02) |
| Product NDC | 62191-007 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sunscreen, AVOBENZONE, OCTINOXATE |
| Dosage Form Name | EMULSION |
| Route Name | TOPICAL |
| Start Marketing Date | 20020301 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Sunrider Manufacturing L.P. |
| Substance Name | AVOBENZONE; OCTINOXATE |
| Strength Number | .02; .06 |
| Strength Unit | g/g; g/g |
| Pharmaceutical Classes |