BODY ACTION PRODUCTS Butt Eze Benzocaine
- Product NDC
- 70742-286
- 11-digit product format
- 707420286
- Labeler code
- 70742
- Product ID
- 70742-286_09d78ab6-7257-6e40-e063-6294a90aef3e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BENZOCAINE
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- PRODUCT MAX GROUP INC
- Application
- M015
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-04-29
- 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
- BODY ACTION PRODUCTS Butt Eze Benzocaine
- 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 Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70742-286-00 | BODY ACTION PRODUCTS Butt Eze Benzocaine | 60 mL in 1 BOTTLE | GEL | 60 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70742-286 | BODY ACTION PRODUCTS BUTT EZE BENZOCAINE (BENZOCAINE) GEL [PRODUCT MAX GROUP INC] | 2 | Current NDC, Legacy NDC, 1 package rows | 20231111_ba75b129-7939-4373-91f5-1772976e6d61.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70742-286-00 | 70742028600 | 60 mL in 1 BOTTLE (70742-286-00) | 60 ml | 2022-04-29 | 0000-00-00 | No | No | Current |