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NDC 58657-0472-12 Sodium Sulfacetamide and Sulfur 100; 50 mg/g; mg/g Details
Sodium Sulfacetamide and Sulfur 100; 50 mg/g; mg/g
Sodium Sulfacetamide and Sulfur is a TOPICAL LIQUID in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Method Pharmaceuticals, LLC. The primary component is SULFACETAMIDE SODIUM; SULFUR.
Product Information
| NDC | 58657-0472 |
|---|---|
| Product ID | 58657-472_0c59c0f1-3ba6-c948-e063-6394a90a04e6 |
| Associated GPIs | 90059903200927 |
| GCN Sequence Number | 045670 |
| GCN Sequence Number Description | sulfacetamide sodium/sulfur CLEANSER 10-5%(W/W) TOPICAL |
| HIC3 | Q5S |
| HIC3 Description | TOPICAL SULFONAMIDES |
| GCN | 48810 |
| HICL Sequence Number | 003344 |
| HICL Sequence Number Description | SULFACETAMIDE SODIUM/SULFUR |
| Brand/Generic | Generic |
| Proprietary Name | Sodium Sulfacetamide and Sulfur |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | SULFACETAMIDE SODIUM, SULFUR |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | LIQUID |
| Route | TOPICAL |
| Active Ingredient Strength | 100; 50 |
| Active Ingredient Units | mg/g; mg/g |
| Substance Name | SULFACETAMIDE SODIUM; SULFUR |
| Labeler Name | Method Pharmaceuticals, LLC |
| Pharmaceutical Class | Sulfonamide Antibacterial [EPC], Sulfonamides [CS] |
| DEA Schedule | n/a |
| Marketing Category | UNAPPROVED DRUG OTHER |
| Application Number | n/a |
| Listing Certified Through | 2024-12-31 |
Package
NDC 58657-0472-12 (58657047212)
| NDC Package Code | 58657-472-12 |
|---|---|
| Billing NDC | 58657047212 |
| Package | 340 g in 1 BOTTLE, PLASTIC (58657-472-12) |
| Marketing Start Date | 2021-11-15 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |