No Rush Desensitizing
- Product NDC
- 71683-010
- 11-digit product format
- 716830010
- Labeler code
- 71683
- Product ID
- 71683-010_5d30fc02-1deb-3d5d-e063-6394a90a04af
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzocaine
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- CC Wellness LLC
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-09-03
- Substance
- BENZOCAINE
- Active strength
- 7.5 g/100mL
- Pharmacologic classes
- Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
- 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
- No Rush Desensitizing
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| BENZOCAINE | 7.5 g/100mL |
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 |
|---|---|---|---|---|---|---|---|
| 71683-010-02 | 71683001002 | 60 mL in 1 BOTTLE, SPRAY (71683-010-02) | 60 ml | 2024-09-03 | No | No | Current |