Home NDC 69681-432 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 Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
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 UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination U3RSY48JW5 Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Preboost BENZOCAINE The Female Health Company d/b/a Veru Healthcare 155e4ba2-7f06-454e-ae7e-e55ef8f891e3 2017-04-07 Warnings Exact identifier ndc (product): 69681-432
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