Iodent Oral Analgesic
- Product NDC
- 65923-094
- 11-digit product format
- 659230094
- Labeler code
- 65923
- Product ID
- 65923-094_4262e1af-6041-bc2d-e063-6294a90a006f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzocaine
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- United Exchange Corp.
- Application
- M022
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2018-01-02
- Substance
- BENZOCAINE
- Active strength
- 200 mg/g
- 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
- Iodent Oral Analgesic
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZOCAINE | 200 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | U3RSY48JW5 |
| Rxcui | 238910 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 65923-094-11 | Iodent Oral Analgesic | 11.9 g in 1 TUBE | GEL | 11.9 | | 8 |
| 65923-094-11 | Iodent Oral Analgesic | 1 in 1 CARTON | GEL | 1 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 65923-094 | IODENT ORAL ANALGESIC (BENZOCAINE) GEL [UNITED EXCHANGE CORP.] | 7 | Current NDC, Legacy NDC, 2 package rows | 20241215_63902125-f8dc-0ada-e053-2991aa0a7ce5.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 65923-094-11 | 65923009411 | 1 TUBE in 1 CARTON (65923-094-11) / 11.9 g in 1 TUBE | 1 tube | 2018-01-02 | 0000-00-00 | No | No | Current |