| Product NDC: | 75936-118 |
| Proprietary Name: | Supergoop |
| Non Proprietary Name: | Avobenzone, Octinoxate, Octisalate |
| Active Ingredient(s): | .44; 1.11; .74 mL/14.79mL; mL/14.79mL; mL/14.79mL & nbsp; Avobenzone, Octinoxate, Octisalate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 75936-118 |
| Labeler Name: | TAYLOR JAMES, LTD. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120628 |
| Package NDC: | 75936-118-01 |
| Package Description: | 14.79 mL in 1 TUBE (75936-118-01) |
| NDC Code | 75936-118-01 |
| Proprietary Name | Supergoop |
| Package Description | 14.79 mL in 1 TUBE (75936-118-01) |
| Product NDC | 75936-118 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Octinoxate, Octisalate |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20120628 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | TAYLOR JAMES, LTD. |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE |
| Strength Number | .44; 1.11; .74 |
| Strength Unit | mL/14.79mL; mL/14.79mL; mL/14.79mL |
| Pharmaceutical Classes |