Home NDC 66096-800 Borax
Product NDC 66096-800
11-digit product format 660960800
Labeler code 66096
Product ID 66096-800_d450f5ab-364d-46cd-e053-2995a90addd1
Type HUMAN OTC DRUG
Nonproprietary name BORAX
Dosage form PELLET
Route ORAL
Labeler OHM PHARMA INC.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2019-11-01
Substance SODIUM BORATE
Active strength 6 [hp_C]/6[hp_C]
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 6 [hp_C]/6[hp_C]
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 66096-800-01 Borax 6 [hp_C] in 1 TUBE PELLET 6 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 66096-800 BORAX PELLET [OHM PHARMA INC.] 4 Current NDC, Legacy NDC, 1 package rows 20211230_2d5f7e06-1195-4ff9-a1e6-cf64c4f7cc4d.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 Marketing start Marketing end Sample Exclude flag Status 66096-800-01 66096080001 6 [hp_C] in 1 TUBE (66096-800-01) 2019-11-01 0000-00-00 No No Current