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Glytone Acne treatment
Glytone Acne treatment - 64760-210-02 - (sulfur)
Drug Information of Glytone Acne treatment
| Product NDC: | 64760-210 |
| Proprietary Name: | Glytone Acne treatment |
| Non Proprietary Name: | sulfur |
| Active Ingredient(s): | 9 g/141g & nbsp; sulfur |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Glytone Acne treatment
| Product NDC: | 64760-210 |
| Labeler Name: | Glytone |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358H |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100301 |
Package Information of Glytone Acne treatment
| Package NDC: | 64760-210-02 |
| Package Description: | 1 TUBE in 1 BOX (64760-210-02) > 50 g in 1 TUBE |
NDC Information of Glytone Acne treatment
| NDC Code | 64760-210-02 |
| Proprietary Name | Glytone Acne treatment |
| Package Description | 1 TUBE in 1 BOX (64760-210-02) > 50 g in 1 TUBE |
| Product NDC | 64760-210 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | sulfur |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100301 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Glytone |
| Substance Name | SULFUR |
| Strength Number | 9 |
| Strength Unit | g/141g |
| Pharmaceutical Classes |
