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NuGLOW
NuGLOW - 65113-8503-3 - (AVOBENZONE, OCTINOXATE, and ZINC OXIDE)
Drug Information of NuGLOW
| Product NDC: | 65113-8503 |
| Proprietary Name: | NuGLOW |
| Non Proprietary Name: | AVOBENZONE, OCTINOXATE, and ZINC OXIDE |
| Active Ingredient(s): | 1; 7; 4 g/100g; g/100g; g/100g & nbsp; AVOBENZONE, OCTINOXATE, and ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NuGLOW
| Product NDC: | 65113-8503 |
| Labeler Name: | G.S. COSMECEUTICAL USA, INC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20101015 |
Package Information of NuGLOW
| Package NDC: | 65113-8503-3 |
| Package Description: | 34 g in 1 JAR (65113-8503-3) |
NDC Information of NuGLOW
| NDC Code | 65113-8503-3 |
| Proprietary Name | NuGLOW |
| Package Description | 34 g in 1 JAR (65113-8503-3) |
| Product NDC | 65113-8503 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | AVOBENZONE, OCTINOXATE, and ZINC OXIDE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20101015 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | G.S. COSMECEUTICAL USA, INC. |
| Substance Name | AVOBENZONE; OCTINOXATE; ZINC OXIDE |
| Strength Number | 1; 7; 4 |
| Strength Unit | g/100g; g/100g; g/100g |
| Pharmaceutical Classes |
