| 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: | 11410-749-03 |
| Package Description: | 15 mL in 1 TUBE (11410-749-03) |
| NDC Code | 11410-749-03 |
| Proprietary Name | In An Instant |
| Package Description | 15 mL in 1 TUBE (11410-749-03) |
| 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 |