Preboost
- Product NDC
- 69681-432
- 11-digit product format
- 696810432
- Labeler code
- 69681
- Product ID
- 69681-432_036fa5d4-a566-486a-aa26-c9a3f01fbcfe
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- benzocaine
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- The Female Health Company d/b/a Veru Healthcare
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2015-03-30
- Substance
- BENZOCAINE
- Active strength
- 4 g/100mL
- 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
- Preboost
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZOCAINE | 4 g/100mL |
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 |
|---|
| 69681-432-10 | Preboost | 10 in 1 BOX | LIQUID | 10 | | 3 |
| 69681-432-10 | Preboost | 1.2 mL in 1 PACKET | LIQUID | 1.2 | | 3 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69681-432 | PREBOOST (BENZOCAINE) LIQUID [THE FEMALE HEALTH COMPANY D/B/A VERU HEALTHCARE] | 3 | Current NDC, Legacy NDC, 2 package rows | 20170407_155e4ba2-7f06-454e-ae7e-e55ef8f891e3.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69681-432-10 | 69681043210 | 10 PACKET in 1 BOX (69681-432-10) / 1.2 mL in 1 PACKET | 10 packet | 2017-04-05 | 0000-00-00 | No | No | Current |