Home
>
National Drug Code (NDC)
>
Dr. Scholls
Dr. Scholls - 11523-7214-1 - (Sodium Sulfide)
Drug Information of Dr. Scholls
| Product NDC: | 11523-7214 |
| Proprietary Name: | Dr. Scholls |
| Non Proprietary Name: | Sodium Sulfide |
| Active Ingredient(s): | 10 mg/g & nbsp; Sodium Sulfide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dr. Scholls
| Product NDC: | 11523-7214 |
| Labeler Name: | MSD Consumer Care, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358D |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20030507 |
Package Information of Dr. Scholls
| Package NDC: | 11523-7214-1 |
| Package Description: | 1 TUBE in 1 CARTON (11523-7214-1) > 8.5 g in 1 TUBE |
NDC Information of Dr. Scholls
| NDC Code | 11523-7214-1 |
| Proprietary Name | Dr. Scholls |
| Package Description | 1 TUBE in 1 CARTON (11523-7214-1) > 8.5 g in 1 TUBE |
| Product NDC | 11523-7214 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sodium Sulfide |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20030507 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | MSD Consumer Care, Inc. |
| Substance Name | SODIUM SULFIDE |
| Strength Number | 10 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
