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ReCreate Foundation
ReCreate Foundation - 51060-009-29 - (Octinoxate, Octisalate, and Oxybenzone)
Drug Information of ReCreate Foundation
| Product NDC: | 51060-009 |
| Proprietary Name: | ReCreate Foundation |
| Non Proprietary Name: | Octinoxate, Octisalate, and Oxybenzone |
| Active Ingredient(s): | 2.2125; 1.18; .59 mL/29.5mL; mL/29.5mL; mL/29.5mL & nbsp; Octinoxate, Octisalate, and Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ReCreate Foundation
| Product NDC: | 51060-009 |
| Labeler Name: | Tarte Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100601 |
Package Information of ReCreate Foundation
| Package NDC: | 51060-009-29 |
| Package Description: | 1 BOTTLE, PUMP in 1 CARTON (51060-009-29) > 29.5 mL in 1 BOTTLE, PUMP |
NDC Information of ReCreate Foundation
| NDC Code | 51060-009-29 |
| Proprietary Name | ReCreate Foundation |
| Package Description | 1 BOTTLE, PUMP in 1 CARTON (51060-009-29) > 29.5 mL in 1 BOTTLE, PUMP |
| Product NDC | 51060-009 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate, Octisalate, and Oxybenzone |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100601 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Tarte Inc |
| Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | 2.2125; 1.18; .59 |
| Strength Unit | mL/29.5mL; mL/29.5mL; mL/29.5mL |
| Pharmaceutical Classes |
