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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| U3RSY48JW5 | BENZOCAINE | 94-09-7 | BENZOCAINE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | 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 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| PREBOOST ® | The Female Health Company d/b/a Veru Healthcare | Safetec of America, Inc. | 2017-04-07 | HUMAN OTC DRUG LABEL | 3 |