NDC 15631-0541

BORAX

Borax

BORAX is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Rxhomeo Private Limited D.b.a. Rxhomeo, Inc. The primary component is Sodium Borate.

Product ID15631-0541_31e32279-1a8f-46a9-a0f5-2b8b3f1794c1
NDC15631-0541
Product TypeHuman Otc Drug
Proprietary NameBORAX
Generic NameBorax
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-12-30
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameSODIUM BORATE
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0541-1

4 TABLET in 1 BLISTER PACK (15631-0541-1)
Marketing Start Date2015-12-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0541-0 [15631054100]

BORAX TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0541-5 [15631054105]

BORAX TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0541-7 [15631054107]

BORAX TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0541-6 [15631054106]

BORAX TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0541-2 [15631054102]

BORAX TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0541-1 [15631054101]

BORAX TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0541-3 [15631054103]

BORAX TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0541-4 [15631054104]

BORAX TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
SODIUM BORATE1 [hp_X]/1

OpenFDA Data

SPL SET ID:15575325-1ae7-4694-b4f7-970581cba7d8
Manufacturer
UNII
UPC Code
  • 8907460005526

    • NDC Crossover Matching brand name "BORAX" or generic name "Borax"

    NDCBrand NameGeneric Name
    0220-0876BoraxSODIUM BORATE
    0220-0877BoraxSODIUM BORATE
    0220-0880BoraxSODIUM BORATE
    0220-0881BoraxSODIUM BORATE
    0220-0884BoraxSODIUM BORATE
    0220-0885BoraxSODIUM BORATE
    0220-0887BoraxSODIUM BORATE
    0220-0888BoraxSODIUM BORATE
    0220-0889BoraxSODIUM BORATE
    0220-0892BoraxSODIUM BORATE
    0360-0070BORAXBORAX
    0360-0071BORAXBORAX
    15631-0084BORAXBORAX
    15631-0541BORAXBORAX
    60512-6205BORAXBORAX
    62106-4925BORAXSodium borate
    63545-506BoraxBorax
    63545-507BoraxBorax
    63545-508BoraxBorax
    63545-509BoraxBorax
    63545-510BoraxBorax
    63545-511BoraxBorax
    63545-512BoraxBorax
    66096-800BoraxBORAX
    68428-261BoraxSODIUM BORATE
    71919-127BoraxSODIUM BORATE
    76472-1134BoraxSODIUM BORATE
    76472-3006BoraxSODIUM BORATE
    76472-4006BoraxSODIUM BORATE
    79718-1023BoraxBorax
    79718-1164BoraxBorax
    69152-1071Borax 30CBorax

    Trademark Results [BORAX]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    BORAX
    BORAX
    74563211 2070225 Live/Registered
    U.S. Borax Inc.
    1994-08-15
    © 2025 FDA.report
    This site is not affiliated with or endorsed by the FDA.