NDC 54973-3111

NAT SULPH

Sodium Sulfate Anhydrous

NAT SULPH is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Hyland's. The primary component is Sodium Sulfate Anhydrous.

• Product ID: 54973-3111_6063eb3d-72b1-d31a-e053-2a91aa0a9696
• NDC: 54973-3111
• Product Type: Human Otc Drug
• Proprietary Name: NAT SULPH
• Generic Name: Sodium Sulfate Anhydrous
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 1940-01-01
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Hyland's
• Substance Name: SODIUM SULFATE ANHYDROUS
• Active Ingredient Strength: 30 [hp_X]/1
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 54973-3111-1

500 TABLET in 1 BOTTLE, PLASTIC (54973-3111-1)

• Marketing Start Date: 1940-01-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 54973-3111-2 [54973311102]

NAT SULPH TABLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1940-01-01
• Marketing End Date: 2017-12-31

NDC 54973-3111-1 [54973311101]

NAT SULPH TABLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1940-01-01

Drug Details

Active Ingredients

Ingredient	Strength
SODIUM SULFATE ANHYDROUS	30 [hp_X]/1

OpenFDA Data

• SPL SET ID: 34cdd03a-e057-43bd-8713-a875c8447bea
• Manufacturer:
  • Hyland's
• UNII:
  • 36KCS0R750
• UPC Code:
  • 0354973311114

NDC Crossover Matching brand name "NAT SULPH" or generic name "Sodium Sulfate Anhydrous"

NDC	Brand Name	Generic Name
54973-3111	NAT SULPH	sodium sulfate anhydrous
54973-4082	Nat Sulph	SODIUM SULFATE
54973-6440	NAT SULPH	sodium sulfate anhydrous
82969-1011	Bestmade Natural Products Nat Sulph	Nat Sulph