Home NDC 85775-112 BVibe Spearmint Deep Throat
Product NDC 85775-112
11-digit product format 857750112
Labeler code 85775
Product ID 85775-112_5ca180e8-39c5-15ad-e063-6294a90a1fbc
Type HUMAN OTC DRUG
Nonproprietary name Benzocaine Numbing Spray
Dosage form LIQUID
Route TOPICAL
Labeler COTR Inc
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-07-15
Substance BENZOCAINE
Active strength 25 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 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 BVibe Spearmint Deep Throat
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZOCAINE 25 mg/mL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 85775-112-11 BVibe Spearmint Deep Throat 59 mL in 1 BOTTLE, SPRAY LIQUID 59 3
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 18 of 153 · 3,057 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 85775-112-11 85775011211 59 mL in 1 BOTTLE, SPRAY (85775-112-11) 59 ml 2025-07-15 No No Current