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 |