Borax

Product NDC
76472-3006
11-digit product format
764723006
Labeler code
76472
Product ID
76472-3006_2dcc6b58-7a86-e2ac-e063-6294a90a9262
Type
HUMAN OTC DRUG
Nonproprietary name
SODIUM BORATE
Dosage form
PELLET
Route
SUBLINGUAL
Labeler
SEVENE USA
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2011-11-30
Substance
SODIUM BORATE
Active strength
200 [kp_C]/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 6 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCSnapshotSource SHA-256
2025-02-02 03:52 UTC · source 2025-01-31excluded productproduct302b2466d912…e7b80fea0513…
2025-02-02 03:52 UTC · source 2025-01-31excluded packagepackage76472-3006-1302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20excluded productproducted331223b511…672a5bd82f5f…
2025-01-20 13:05 UTC · source 2025-01-20excluded packagepackage76472-3006-1ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-10excluded productproduct0efc9e666f02…f202fb6c5f17…
2025-01-11 03:41 UTC · source 2025-01-10excluded packagepackage76472-3006-10efc9e666f02…f202fb6c5f17…

Additional Listing Data#

Finished product
Yes
Brand name base
Borax
Brand name suffix
200ck
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SODIUM BORATE200 [kp_C]/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
91MBZ8H3QOInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
c8d359b2-3ba0-3117-e053-2a95a90aac2fAvailable on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76472-3006-12025-02-10C16284748780-12cef2736-6d08-d83d-e063-dadaa90ab31fSevene USA (as PLD) - BORAX 200ck (76472-3006)
76472-3006-12025-01-30C16284748780-12cef2736-6d08-d83d-e063-dadaa90ab31fSevene USA (as PLD) - BORAX 200ck (76472-3006)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76472-3006-1Borax200ck80 in 1 CYLINDERPELLET804

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76472-3006BORAX 200CK (SODIUM BORATE) PELLET [SEVENE USA]4Current NDC, Legacy NDC, 1 package rows20250212_c8d359b2-3ba0-3117-e053-2a95a90aac2f.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
Borax 200ckSODIUM BORATESEVENE USAc8d359b2-3ba0-3117-e053-2a95a90aac2f2025-02-10WarningsExact identifier
ndc (product): 76472-3006

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
76472-3006-17647230060180 PELLET in 1 CYLINDER (76472-3006-1) 80 pellet2011-11-300000-00-00NoNoCurrent