Label: BVIBE SPEARMINT DEEP THROAT- benzocaine numbing spray liquid
- NDC Code(s): 85775-112-11
- Packager: COTR Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated August 22, 2025
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient(s)
- Purpose
- Use
-
Warnings
For external use only. Do not apply to genitals or other body parts.
Allergy Alert: Avoid if allergic to benzocaine or other local anesthetics (e.g., lidocaine, procaine)
Do Not Use: If you have a history of methemoglobinemia or take related medications (e.g., nitrates, sulfonamides).
On irritated or broken mucous membranes.
When Using: Avoid eyes/nostrils; rinse if contact occurs.
Do not swallow immediately; allow throat numbing.
Avoid eating/drinking for 1 hour post-use to prevent choking.
Seek immediate medical help for excessive numbness, breathing issues, dizziness, or bluish skin.Stop Use and Consult a Doctor If: Severe burning, swelling, irritation, rash, or prolonged numbing (>1-2 hours) occurs.
Ask a Doctor Before Use If: You have respiratory, heart, or liver issues, are pregnant/breastfeeding, or take interacting medications.
Keep Out of Reach of Children: Contact Poison Control
(1-800-222-1222) if swallowed.
• Other Warnings: Overuse may increase methemoglobinemia risk.
Avoid continuous/large - KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
- Package Label - Principal Display Panel
-
INGREDIENTS AND APPEARANCE
BVIBE SPEARMINT DEEP THROAT
benzocaine numbing spray liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:85775-112 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE 25 mg in 1 mL Inactive Ingredients Ingredient Name Strength ACESULFAME POTASSIUM (UNII: 23OV73Q5G9) SUCRALOSE (UNII: 96K6UQ3ZD4) ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) CITRIC ACID (UNII: 2968PHW8QP) SODIUM BENZOATE (UNII: OJ245FE5EU) SPEARMINT (UNII: J7I2T6IV1N) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:85775-112-11 59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 07/15/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 07/15/2025 Labeler - COTR Inc (080923922)

