Home NDC 76472-1134 Borax
Product NDC 76472-1134
11-digit product format 764721134
Labeler code 76472
Product ID 76472-1134_0fa4e7df-771f-3984-e063-6394a90abf72
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 30 [hp_C]/1
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Borax
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM BORATE 30 [hp_C]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 91MBZ8H3QO Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 76472-1134-1 Borax 80 in 1 CYLINDER PELLET 80 26
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 76472-1134 BORAX (SODIUM BORATE) PELLET [SEVENE USA] 26 Current NDC, Legacy NDC, 1 package rows 20240127_2c24fcda-dcf9-41be-9788-10833d53ab38.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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 76472-1134-1 76472113401 80 PELLET in 1 CYLINDER (76472-1134-1) 80 pellet 2011-11-30 0000-00-00 No No Current