COTR-PLP Delay Spray

Manufacturer
COTR Inc
Effective date
2026-09-29
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-10-01 14:01:37

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 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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
070fbed5-7088-434a-a7ce-f2a64d8d40acProduct name220260107
bee66ce1-adb7-9d3b-67d9-582e4c54e80fProduct name520250819
860a93dc-4863-49cc-b284-6bbe8191bc48Product name420250214
eaba870a-6a9d-442e-8643-87b3f558a451Product name120250117
9b4cf230-fd05-41d5-98c6-5db9ecb27b86Product name120230117
7d755fa1-1087-4dcd-98f0-6d4bba479a57Product name320210602
aed701d5-9c75-dfaf-7154-cde46179faeaProduct name920200313
fa8b5901-e681-426f-82fe-54f6d81ec698Product name420180619
332d03e4-aa24-4b11-841a-02bf41081920Product name120171221
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070Product name120171221
68ed98f8-24c2-44a0-944a-6d36e82ce25aProduct name120141222
1cd42bc2-a430-c72b-636d-991b235fbf80Product name120140508
49fa150c-f0de-cce7-3d9c-993ed81c5698Product name120140508
4d7ae718-ed00-bae8-2abe-9eaec1eef7ffProduct name120140508
9137811f-f279-8640-5aeb-99fa2145d64dProduct name120140508

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85775-11185775-111-11

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

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12025-07-12full-release2026-06-01 01:07:13

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
BVibeLIDOCAINE HCL DELAY SPRAYCOTR Inc39bfb77f-090a-9ef1-e063-6294a90a56442025-07-12WarningsExact identifier
ndc (package): 85775-111-11
ndc (product): 85775-111
ndc11 (package): 85775011111
spl set id: 39bfb77f-090a-9ef1-e063-6294a90a5644

Reported adverse events (FAERS/openFDA)#

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