BLT 1
- Product NDC
- 70372-727
- 11-digit product format
- 703720727
- Labeler code
- 70372
- Product ID
- 70372-727_4878fc9b-f123-910a-e063-6394a90a7e47
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BENZOCAINE
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- CENTURA PHARMACEUTICALS INC
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2016-10-15
- Substance
- BENZOCAINE
- Active strength
- 20 g/100g
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- BLT 1
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZOCAINE | 20 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | U3RSY48JW5 |
| Rxcui | 244557 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70372-727-01 | BLT 1 | 5 g in 1 POUCH | OINTMENT | 5 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70372-727 | BLT 1 (BENZOCAINE) OINTMENT [CENTURA PHARMACEUTICALS INC] | 7 | Current NDC, Legacy NDC, 1 package rows | 20250129_3eea2171-850b-4045-e054-00144ff8d46c.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 |
|---|
| 70372-727-01 | 70372072701 | 5 g in 1 POUCH (70372-727-01) | 5 g | 2016-10-15 | 0000-00-00 | No | No | Current |