CVS Topical Analgesic Hemorrhoidal
- Product NDC
- 51316-207
- 11-digit product format
- 513160207
- Labeler code
- 51316
- Product ID
- 51316-207_4e0916a9-7c93-eb70-e063-6294a90a11b6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- DIBUCAINE
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- CVS PHARMACY,INC
- Application
- M015
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-02-14
- Substance
- DIBUCAINE
- Active strength
- 10 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- CVS Topical Analgesic Hemorrhoidal
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DIBUCAINE | 10 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L6JW2TJG99 |
| Rxcui | 238784 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51316-207-28 | CVS Topical Analgesic Hemorrhoidal | 28 mL in 1 TUBE | OINTMENT | 28 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 51316-207-28 | 51316020728 | 28 mL in 1 TUBE (51316-207-28) | 28 ml | 2026-02-14 | No | No | Current |