Finafta
- Product NDC
- 65852-001
- 11-digit product format
- 658520001
- Labeler code
- 65852
- Product ID
- 65852-001_3f7c6100-fd2d-9cd9-e063-6294a90a2486
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzocaine
- Dosage form
- SPRAY
- Route
- ORAL
- Labeler
- Dextrum Laboratories Inc.
- Application
- M022
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2004-09-01
- Substance
- BENZOCAINE
- Active strength
- 7.5 mg/100mL
- Pharmacologic classes
- Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Finafta
- Brand name suffix
- MultiOral
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZOCAINE | 7.5 mg/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | U3RSY48JW5 |
| Rxcui | 1110816, 1110820 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 65852-001-02 | FinaftaMultiOral | 1 in 1 CARTON | SPRAY | 1 | | 1 |
| 65852-001-02 | FinaftaMultiOral | 59 mL in 1 BOTTLE, SPRAY | SPRAY | 59 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 65852-001-02 | 65852000102 | 1 BOTTLE, SPRAY in 1 CARTON (65852-001-02) / 59 mL in 1 BOTTLE, SPRAY | 2004-09-01 | No | No | Historical |