DC Blister Booster Adult
- Product NDC
- 84035-014
- 11-digit product format
- 840350014
- Labeler code
- 84035
- Product ID
- 84035-014_5bcbf59b-9b2e-1a9e-e063-6294a90a7017
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Fluoride 0.24%
- Dosage form
- KIT
- Route
- DENTAL
- Labeler
- Rabbit Ind�stria e Com�rcio de Produtos de Higiene Pessoal Ltda
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-09-01
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- DC Blister Booster Adult
- Listing expiration
- 2027-12-31
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 84035-014-20 | 84035001420 | 1 KIT in 1 BLISTER PACK (84035-014-20) * 1 TUBE in 1 CARTON (84035-006-20) / 20 g in 1 TUBE | 1 kit | 2026-09-01 | No | No | Current |