Anticavity
- Product NDC
- 21130-435
- 11-digit product format
- 211300435
- Labeler code
- 21130
- Product ID
- 21130-435_d53601ed-f05b-4f4e-9ca0-5f894ad2956a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium fluoride
- Dosage form
- MOUTHWASH
- Route
- ORAL
- Labeler
- LIVING BETTER BRANDS LLC
- Application
- part355
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2015-09-09
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 0 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21130-435 | ANTICAVITY (SODIUM FLUORIDE) MOUTHWASH [LIVING BETTER BRANDS LLC] | 4 | Legacy NDC | 20250313_5f1ffe30-dd29-47ab-87fe-03b51b136dd8.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 21130-435-45 | 21130043545 | 946 mL in 1 BOTTLE, PLASTIC (21130-435-45) | 946 ml | 2015-09-09 | 0000-00-00 | No | No | Current |