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DHC Acne Spot Therapy
DHC Acne Spot Therapy - 63433-897-10 - (Sulfur)
Drug Information of DHC Acne Spot Therapy
| Product NDC: | 63433-897 |
| Proprietary Name: | DHC Acne Spot Therapy |
| Non Proprietary Name: | Sulfur |
| Active Ingredient(s): | 6 mg/.2g & nbsp; Sulfur |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DHC Acne Spot Therapy
| Product NDC: | 63433-897 |
| Labeler Name: | DHC USA Incorporated |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110801 |
Package Information of DHC Acne Spot Therapy
| Package NDC: | 63433-897-10 |
| Package Description: | 1 g in 1 CELLO PACK (63433-897-10) |
NDC Information of DHC Acne Spot Therapy
| NDC Code | 63433-897-10 |
| Proprietary Name | DHC Acne Spot Therapy |
| Package Description | 1 g in 1 CELLO PACK (63433-897-10) |
| Product NDC | 63433-897 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sulfur |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110801 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | DHC USA Incorporated |
| Substance Name | SULFUR |
| Strength Number | 6 |
| Strength Unit | mg/.2g |
| Pharmaceutical Classes |
