Product NDC: | 11410-749 |
Proprietary Name: | In An Instant |
Non Proprietary Name: | Octinoxate, Octisalate, and Avobenzone |
Active Ingredient(s): | .02; .075; .05 mg/mL; mL/mL; mL/mL & nbsp; Octinoxate, Octisalate, and Avobenzone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 11410-749 |
Labeler Name: | Guthy-Renker LLC. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20071025 |
Package NDC: | 11410-749-17 |
Package Description: | 50 mL in 1 TUBE (11410-749-17) |
NDC Code | 11410-749-17 |
Proprietary Name | In An Instant |
Package Description | 50 mL in 1 TUBE (11410-749-17) |
Product NDC | 11410-749 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octinoxate, Octisalate, and Avobenzone |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20071025 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Guthy-Renker LLC. |
Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE |
Strength Number | .02; .075; .05 |
Strength Unit | mg/mL; mL/mL; mL/mL |
Pharmaceutical Classes |