United Dental Kit
- Product NDC
- 42509-134
- 11-digit product format
- 425090134
- Labeler code
- 42509
- Product ID
- 42509-134_08aaf4ce-9b3c-5491-e063-6294a90a8a4e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SODIUM MONOFLUOROPHOSPHATE
- Dosage form
- KIT
- Labeler
- Wessco International
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-06-01
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- United Dental Kit
- 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 |
|---|
| 42509-134-01 | United Dental Kit | 1 in 1 KIT | KIT | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 42509-134 | UNITED DENTAL KIT (SODIUM MONOFLUOROPHOSPHATE) KIT [WESSCO INTERNATIONAL] | 2 | Current NDC, 1 package rows | 20231027_7f348fe7-9918-4934-bed0-f0a77c09d046.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 42509-134-01 | 42509013401 | 1 KIT in 1 KIT (42509-134-01) * 5 g in 1 TUBE (42555-060-94) | 1 kit | 2023-06-01 | No | No | Historical |