WHITE GLO BIO-ENZYME
- Product NDC
- 73656-005
- 11-digit product format
- 736560005
- Labeler code
- 73656
- Product ID
- 73656-005_2f18bf4f-05b2-3f57-e063-6394a90aa4aa
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SODIUM MONOFLUOROPHOSPHATE
- Dosage form
- KIT
- Labeler
- WHITE GLO USA INC
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-02-15
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- WHITE GLO BIO-ENZYME
- Listing expiration
- 2026-12-31
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Rxcui | 545626 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 73656-005-00 | WHITE GLO BIO-ENZYME | 1 in 1 KIT | KIT | 1 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 73656-005 | WHITE GLO BIO-ENZYME (SODIUM MONOFLUOROPHOSPHATE) KIT [WHITE GLO USA INC] | 6 | Current NDC, Legacy NDC, 1 package rows | 20250228_f894a841-0df7-470d-8fc2-c9d6ba0edf99.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 73656-005-00 | 73656000500 | 1 KIT in 1 KIT (73656-005-00) * 150 g in 1 TUBE (73656-006-00) | 1 kit | 2020-02-15 | 0000-00-00 | No | No | Current |