FDA.reportPublic FDA data

NAT SULPH

Product NDC
54973-6440
11-digit product format
549736440
Labeler code
54973
Product ID
54973-6440_f03141f6-9def-7d57-e053-2995a90a16ae
Type
HUMAN OTC DRUG
Nonproprietary name
sodium sulfate anhydrous
Dosage form
TABLET
Route
ORAL
Labeler
Hyland's Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1940-01-01
Substance
SODIUM SULFATE ANHYDROUS
Active strength
6 [hp_X]/1
Pharmacologic classes
Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
NAT SULPH
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SODIUM SULFATE ANHYDROUS6 [hp_X]/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
36KCS0R750Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
84d12830-b34f-415d-a19a-947c5040d8bfAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
95250459-30e4-45c1-b08a-993044f49109Product name220250805
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
a21a21e5-f36d-4c1f-8918-def921b8f7e3Product name320250124
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54973-6440-1NAT SULPH500 in 1 BOTTLE, PLASTICTABLET5003
54973-6440-2NAT SULPH1000 in 1 BOTTLE, PLASTICTABLET10003

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
SODIUM SULFATE ANHYDROUSACTIVE INGREDIENT36KCS0R750NAT SULPH (SODIUM SULFATE ANHYDROUS) TABLET [HYLAND'S]1
SODIUM SULFATE ANHYDROUSACTIVE MOIETY36KCS0R750NAT SULPH (SODIUM SULFATE ANHYDROUS) TABLET [HYLAND'S]1
ACACIAINACTIVE INGREDIENT5C5403N26ONAT SULPH (SODIUM SULFATE ANHYDROUS) TABLET [HYLAND'S]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GNAT SULPH (SODIUM SULFATE ANHYDROUS) TABLET [HYLAND'S]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54973-6440NAT SULPH (SODIUM SULFATE ANHYDROUS) TABLET [HYLAND'S INC.]3Current NDC, Legacy NDC, 2 package rows20221220_84d12830-b34f-415d-a19a-947c5040d8bf.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
NAT SULPHSODIUM SULFATE ANHYDROUSHyland's Inc.84d12830-b34f-415d-a19a-947c5040d8bf2022-12-19WarningsExact identifier
ndc (product): 54973-6440

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
54973-6440-154973644001500 TABLET in 1 BOTTLE, PLASTIC (54973-6440-1) 500 tablet1940-01-010000-00-00NoNoCurrent
54973-6440-2549736440021000 TABLET in 1 BOTTLE, PLASTIC (54973-6440-2) 1000 tablet1940-01-010000-00-00NoNoCurrent