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 Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 91MBZ8H3QO |
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 |
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 |