NDC 15631-0084
BORAX
Borax
BORAX is a Oral Pellet 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 ID | 15631-0084_470993b5-1151-4839-9243-b652519bb9ca |
| NDC | 15631-0084 |
| Product Type | Human Otc Drug |
| Proprietary Name | BORAX |
| Generic Name | Borax |
| Dosage Form | Pellet |
| Route of Administration | ORAL |
| Marketing Start Date | 2015-09-12 |
| Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
| Labeler Name | Rxhomeo Private Limited d.b.a. Rxhomeo, Inc |
| Substance Name | SODIUM BORATE |
| Active Ingredient Strength | 1 [hp_X]/1 |
| NDC Exclude Flag | E |
| Listing Certified Through | 2018-12-31 |
Packaging
NDC 15631-0084-0
100 PELLET in 1 PACKAGE (15631-0084-0)
| Marketing Start Date | 2018-01-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 15631-0084-1 [15631008401]
BORAX PELLET
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-01-01 |
| Inactivation Date | 2020-01-31 |
| Reactivation Date | 2020-02-19 |
NDC 15631-0084-4 [15631008404]
BORAX PELLET
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-01-01 |
| Inactivation Date | 2020-01-31 |
| Reactivation Date | 2020-02-19 |
NDC 15631-0084-0 [15631008400]
BORAX PELLET
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-01-01 |
| Inactivation Date | 2020-01-31 |
| Reactivation Date | 2020-02-19 |
NDC 15631-0084-2 [15631008402]
BORAX PELLET
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-01-01 |
| Inactivation Date | 2020-01-31 |
| Reactivation Date | 2020-02-19 |
NDC 15631-0084-5 [15631008405]
BORAX PELLET
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-01-01 |
| Inactivation Date | 2020-01-31 |
| Reactivation Date | 2020-02-19 |
NDC 15631-0084-3 [15631008403]
BORAX PELLET
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-01-01 |
| Inactivation Date | 2020-01-31 |
| Reactivation Date | 2020-02-19 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| SODIUM BORATE | 1 [hp_X]/1 |
OpenFDA Data
| SPL SET ID: | a3d8768d-6fd9-4a7d-9143-5397308fa331 |
| Manufacturer | |
| UNII |
NDC Crossover Matching brand name "BORAX" or generic name "Borax"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0220-0876 | Borax | SODIUM BORATE |
| 0220-0877 | Borax | SODIUM BORATE |
| 0220-0880 | Borax | SODIUM BORATE |
| 0220-0881 | Borax | SODIUM BORATE |
| 0220-0884 | Borax | SODIUM BORATE |
| 0220-0885 | Borax | SODIUM BORATE |
| 0220-0887 | Borax | SODIUM BORATE |
| 0220-0888 | Borax | SODIUM BORATE |
| 0220-0889 | Borax | SODIUM BORATE |
| 0220-0892 | Borax | SODIUM BORATE |
| 0360-0070 | BORAX | BORAX |
| 0360-0071 | BORAX | BORAX |
| 15631-0084 | BORAX | BORAX |
| 15631-0541 | BORAX | BORAX |
| 60512-6205 | BORAX | BORAX |
| 62106-4925 | BORAX | Sodium borate |
| 63545-506 | Borax | Borax |
| 63545-507 | Borax | Borax |
| 63545-508 | Borax | Borax |
| 63545-509 | Borax | Borax |
| 63545-510 | Borax | Borax |
| 63545-511 | Borax | Borax |
| 63545-512 | Borax | Borax |
| 66096-800 | Borax | BORAX |
| 68428-261 | Borax | SODIUM BORATE |
| 71919-127 | Borax | SODIUM BORATE |
| 76472-1134 | Borax | SODIUM BORATE |
| 76472-3006 | Borax | SODIUM BORATE |
| 76472-4006 | Borax | SODIUM BORATE |
| 79718-1023 | Borax | Borax |
| 79718-1164 | Borax | Borax |
| 69152-1071 | Borax 30C | Borax |
Trademark Results [BORAX]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 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.