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Bain de Soleil Orange Creme
Bain de Soleil Orange Creme - 11523-7305-2 - (Octinoxate and Oxybenzone)
Drug Information of Bain de Soleil Orange Creme
| Product NDC: | 11523-7305 |
| Proprietary Name: | Bain de Soleil Orange Creme |
| Non Proprietary Name: | Octinoxate and Oxybenzone |
| Active Ingredient(s): | 35; 15 mg/g; mg/g & nbsp; Octinoxate and Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Bain de Soleil Orange Creme
| Product NDC: | 11523-7305 |
| Labeler Name: | Schering-Plough HealthCare Products, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19990521 |
Package Information of Bain de Soleil Orange Creme
| Package NDC: | 11523-7305-2 |
| Package Description: | 1 TUBE in 1 CARTON (11523-7305-2) > 99 g in 1 TUBE (11523-7305-1) |
NDC Information of Bain de Soleil Orange Creme
| NDC Code | 11523-7305-2 |
| Proprietary Name | Bain de Soleil Orange Creme |
| Package Description | 1 TUBE in 1 CARTON (11523-7305-2) > 99 g in 1 TUBE (11523-7305-1) |
| Product NDC | 11523-7305 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate and Oxybenzone |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 19990521 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Schering-Plough HealthCare Products, Inc. |
| Substance Name | OCTINOXATE; OXYBENZONE |
| Strength Number | 35; 15 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |
