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 |