PureLife Topical Anesthetic
- Product NDC
- 68987-001
- 11-digit product format
- 689870001
- Labeler code
- 68987
- Product ID
- 68987-001_2b386f93-586f-d4aa-e063-6394a90a4a47
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzocaine
- Dosage form
- GEL
- Route
- DENTAL
- Labeler
- PureLife Dental
- Application
- M022
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2013-07-01
- 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
- PureLife Topical Anesthetic
- 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 Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68987-001-30 | PureLife Topical Anesthetic | 30 g in 1 JAR | GEL | 30 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68987-001 | PURELIFE TOPICAL ANESTHETIC (BENZOCAINE) GEL [PURELIFE DENTAL] | 5 | Current NDC, Legacy NDC, 1 package rows | 20250110_4e68a4b9-a08c-4360-92b7-53d0f9df092d.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 |
|---|
| 68987-001-30 | 68987000130 | 30 g in 1 JAR (68987-001-30) | 30 g | 2018-10-01 | 0000-00-00 | No | No | Current |