nat sulph

Generic: sodium sulfate anhydrous

Labeler: hyland's inc.
NDC Directory HUMAN OTC DRUG UNAPPROVED HOMEOPATHIC Inactive Finished

Drug Facts

Product Profile

Brand Name nat sulph
Generic Name sodium sulfate anhydrous
Labeler hyland's inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

sodium sulfate anhydrous 6 [hp_X]/1

Manufacturer
Hyland's Inc.

Identifiers & Regulatory

Product NDC 54973-6440
Product ID 54973-6440_f03141f6-9def-7d57-e053-2995a90a16ae
Product Type HUMAN OTC DRUG
Marketing Category UNAPPROVED HOMEOPATHIC
Listing Expiration 2026-12-31
Marketing Start 1940-01-01

Pharmacologic Class

Classes
increased large intestinal motility [pe] inhibition large intestine fluid/electrolyte absorption [pe] osmotic activity [moa] osmotic laxative [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 549736440
Hyphenated Format 54973-6440

Supplemental Identifiers

UPC
0354973644014
UNII
36KCS0R750

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name nat sulph (source: ndc)
Generic Name sodium sulfate anhydrous (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 6 [hp_X]/1
source: ndc
Packaging
  • 500 TABLET in 1 BOTTLE, PLASTIC (54973-6440-1)
  • 1000 TABLET in 1 BOTTLE, PLASTIC (54973-6440-2)
source: ndc

Packages (2)

54973-6440-1 500 TABLET in 1 BOTTLE, PLASTIC (54973-6440-1) 54973-6440-2 1000 TABLET in 1 BOTTLE, PLASTIC (54973-6440-2)

Ingredients (1)

sodium sulfate anhydrous (6 [hp_X]/1)

Linked Drug Pages (1)

NAT SULPH ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f03141f6-9def-7d57-e053-2995a90a16ae", "openfda": {"upc": ["0354973644014"], "unii": ["36KCS0R750"], "spl_set_id": ["84d12830-b34f-415d-a19a-947c5040d8bf"], "manufacturer_name": ["Hyland's Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (54973-6440-1)", "package_ndc": "54973-6440-1", "marketing_start_date": "19400101"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (54973-6440-2)", "package_ndc": "54973-6440-2", "marketing_start_date": "19400101"}], "brand_name": "NAT SULPH", "product_id": "54973-6440_f03141f6-9def-7d57-e053-2995a90a16ae", "dosage_form": "TABLET", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "54973-6440", "generic_name": "sodium sulfate anhydrous", "labeler_name": "Hyland's Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "NAT SULPH", "active_ingredients": [{"name": "SODIUM SULFATE ANHYDROUS", "strength": "6 [hp_X]/1"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19400101", "listing_expiration_date": "20261231"}