NDC 72934-8170

SALICYLIC ACID 2% /SODIUM SULFACETAMIDE MONOHYDRATE 8%

Salicylic Acid 2% /sodium Sulfacetamide Monohydrate 8%

SALICYLIC ACID 2% /SODIUM SULFACETAMIDE MONOHYDRATE 8% is a Topical Suspension in the Human Prescription Drug category. It is labeled and distributed by Sincerus Florida, Llc. The primary component is Sulfacetamide Sodium; Salicylic Acid.

• Product ID: 72934-8170_87390b9e-a525-2e36-e053-2a91aa0affe2
• NDC: 72934-8170
• Product Type: Human Prescription Drug
• Proprietary Name: SALICYLIC ACID 2% /SODIUM SULFACETAMIDE MONOHYDRATE 8%
• Generic Name: Salicylic Acid 2% /sodium Sulfacetamide Monohydrate 8%
• Dosage Form: Suspension
• Route of Administration: TOPICAL
• Marketing Start Date: 2019-05-01
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: Sincerus Florida, LLC
• Substance Name: SULFACETAMIDE SODIUM; SALICYLIC ACID
• Active Ingredient Strength: 8 g/100g; g/100g
• Pharm Classes: Sulfonamide Antibacterial [EPC],Sulfonamides [CS]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 72934-8170-6

120 g in 1 CYLINDER (72934-8170-6)

• Marketing Start Date: 2019-05-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 72934-8170-6 [72934817006]

SALICYLIC ACID 2% /SODIUM SULFACETAMIDE MONOHYDRATE 8% SUSPENSION

• Marketing Category: unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: GM
• Marketing Start Date: 2019-05-01

NDC 72934-8170-7 [72934817007]

SALICYLIC ACID 2% /SODIUM SULFACETAMIDE MONOHYDRATE 8% SUSPENSION

• Marketing Category: unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2019-05-17

Drug Details

Active Ingredients

Ingredient	Strength
SULFACETAMIDE SODIUM	8 g/100g

Pharmacological Class

• Sulfonamide Antibacterial [EPC]
• Sulfonamides [CS]
• Sulfonamide Antibacterial [EPC]
• Sulfonamides [CS]