INTIMALE Benzocaine Delay Gel
- Product NDC
- 81923-369
- 11-digit product format
- 819230369
- Labeler code
- 81923
- Product ID
- 81923-369_0976eff9-48b9-1669-e063-6394a90a8240
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BENZOCAINE
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- SKINS SEXUAL HEALTH LIMITED
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-10-03
- Substance
- BENZOCAINE
- Active strength
- 50 mg/mL
- 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
- INTIMALE Benzocaine Delay Gel
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZOCAINE | 50 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | U3RSY48JW5 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 81923-369-00 | INTIMALE Benzocaine Delay Gel | 15 mL in 1 BOTTLE | GEL | 15 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 81923-369 | INTIMALE BENZOCAINE DELAY GEL (BENZOCAINE) GEL [SKINS SEXUAL HEALTH LIMITED] | 2 | Current NDC, Legacy NDC, 1 package rows | 20231106_b845bfd5-ab73-495f-97ef-e959bc6311d9.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 81923-369-00 | 81923036900 | 15 mL in 1 BOTTLE (81923-369-00) | 15 ml | 2022-10-03 | 0000-00-00 | No | No | Current |