PLP-COTR Delay Spray

Manufacturer
Private Label Productions LLC
Effective date
2025-08-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:34:51

Label at a glance#

ProductBVibe
Active ingredientLIDOCAINE HYDROCHLORIDE
Label structure8 sections

Dosage and administration

Adults: Apply 3-10 sprays to penis head/shaft (focus on frenulum/tip) 10 minutes before intercourse. Start with 3 sprays to assess sensitivity. Shake bottle, spray directly or massage on. Allow 10 minutes absorption; wipe excess before oral sex. Wash off post-intercourse. Store at 68°-77°F, away from heat/sunlight.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Lidocaine HCl 9.94 mg

Purpose

OTC - PURPOSE SECTION

Male Genital Desensitizer Topical Anesthetic

Use

INDICATIONS & USAGE SECTION

Temporarily slows ejaculation onset for premature ejaculation management.

Warnings

WARNINGS SECTION

For external use only.
Allergy alert: Avoid if allergic to lidocaine or other topical anesthetics.
Do Not Use: On broken/irritated/sensitive skin or if partner is pregnant.
When Using: Avoid eye contact; rinse if occurs.
Do not apply excessively to avoid side effects (e.g., numbness, irregular heartbeat).
Discontinue if rash, irritation, or burning occurs.
Stop Use and Consult a Doctor If: No relief, rash, irritation, or excessive numbness occurs.
Ask a Doctor Before Use If: You have liver/kidney issues or take interacting medications.
Keep Out of Reach of Children: Contact Poison Control if swallowed.
Other Warnings: Lidocaine may numb partner's mouth/throat during oral sex; allow 10 minutes absorption or wipe excess.
Overuse (>10 sprays) may cause numbness or erection loss.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of childeren.Contact Poison Control if

Directions

DOSAGE & ADMINISTRATION SECTION

Adults: Apply 3-10 sprays to penis head/shaft (focus on frenulum/tip) 10 minutes before intercourse.
Start with 3 sprays to assess sensitivity.
Shake bottle, spray directly or massage on.
Allow 10 minutes absorption; wipe excess before oral sex.
Wash off post-intercourse.

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified Water, Propanediol, Alcohol, Aloe Barbadensis Leaf Juice, Laureth 9, PEG 8, Panthenol, Panax Ginseng Root Extract, Hydroxyethy|cellulose, Menthyl Lactate, PPG-26-Buteth-26, PEG-40 Hydrogenated Castor Oil, Caprylyl Glycol, Phenoxyethanol, Ethylhexylglycerin

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77632-16277632-162-11

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Source Document#

Source XML

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
3cf6cc19-092f-ba80-e063-6394a90a22dd3cf6cc10-0bb4-b3b2-e063-6394a90a6c5b2025-08-22WarningsExact identifier
spl id: 3cf6cc19-092f-ba80-e063-6394a90a22dd
spl set id: 3cf6cc10-0bb4-b3b2-e063-6394a90a6c5b

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.