BVibe Spearmint Deep Throat by Private Label Productions LLC PLP-COTR Deep Throat

BVibe Spearmint Deep Throat by

Drug Labeling and Warnings

BVibe Spearmint Deep Throat by is a Otc medication manufactured, distributed, or labeled by Private Label Productions LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

BVIBE SPEARMINT DEEP THROAT- benzocaine numbing spray liquid 
Private Label Productions LLC

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PLP-COTR Deep Throat

Active Ingredient(s)

Benzocaine 2.5%

Purpose

Oral Anesthetic

Use

Temporarily reduces gag reflex by desensitizing the throat for deeper oral activity.

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 childeren.Contact Poison Control if

Directions

Adults (18+): 1-2 sprays to throat, max 3-4 per use.
Allow 30-60 seconds before swallowing; wait 1-2 minutes for full effect.
Numbing fades within 1 hour. Max 4 sprays/session, 12 sprays/24 hours.

Store at 68°-77°F, away from heat/sunlight.

Other information

Inactive ingredients

Purified Water, Ethyl Alcohol, Glycerin, Acesulfame Potassium, Sucralose, Flavor, Citric Acid, Sodium Benzoate, Potassium

Package Label - Principal Display Panel

BVIBE SPEARMINT DEEP THROAT 
benzocaine numbing spray liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77632-161
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: 77632-161-11	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 - Private Label Productions LLC (046278265)

Revised: 8/2025

Document Id: 3cf6b956-7807-b5ee-e063-6394a90a38ea

34390-5

Set id: 3cf6b963-150e-b500-e063-6394a90a62ae

Version: 1

Effective Time: 20250822