Sodium Fluoride 1.1% Dental Gel MINT
- Product NDC
- 71085-074
- 11-digit product format
- 710850074
- Labeler code
- 71085
- Product ID
- 71085-074_2c3d902a-c321-d343-e063-6394a90a5ff9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SODIUM FLUORIDE
- Dosage form
- GEL
- Route
- ORAL
- Labeler
- IPG PHARMACEUTICALS, INC.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2025-01-14
- Substance
- SODIUM FLUORIDE
- Active strength
- 1.1 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Sodium Fluoride 1.1% Dental Gel MINT
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM FLUORIDE | 1.1 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 8ZYQ1474W7 |
| Rxcui | 1486566 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71085-074-02 | Sodium Fluoride 1.1% Dental Gel MINT | 1 in 1 CARTON | GEL | 1 | | 1 |
| 71085-074-02 | Sodium Fluoride 1.1% Dental Gel MINT | 200 g in 1 TUBE | GEL | 200 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71085-074 | SODIUM FLUORIDE 1.1% DENTAL GEL MINT (SODIUM FLUORIDE) GEL [IPG PHARMACEUTICALS, INC.] | 1 | Current NDC, 2 package rows | 20250122_a87da661-5b43-41d1-af01-2227a99bc6ab.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 |
|---|
| 71085-074-02 | 71085007402 | 1 TUBE in 1 CARTON (71085-074-02) / 200 g in 1 TUBE | 1 tube | 2025-01-14 | No | No | Current |