MaxGro

Manufacturer
CJH Innovations LLC
Effective date
2025-11-17
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
monthly-update
Hydrated at
2026-06-03 17:40:21

Label at a glance#

ProductMaxGro
Active ingredientLIDOCAINE
Label structure7 sections

Indications and uses

helps in temporarily slowing the onset of ejaculation

Label contents#

Full prescribing information#

Dosage & administration

DOSAGE & ADMINISTRATION SECTION

Gently shake bottle. Hold upright and press pump until spray dispenses. Apply 3 or more sprays, not to exceed 10, to head and shaft of penis 5-15 minutes before intercourse or use as directed by a doctor. Wash product off after intercourse.

Warnings

WARNINGS SECTION

For external use only

Do not use
■ in the eyes
■ over large areas of the body
■ if allergic to any ingredient in this product
■ more than 1 week unless directed by a doctor

Ask a doctor before use if you have
■ any concerns about using this product

When using this product
■ avoid contact with the eyes

Stop use and ask a doctor if
■ condition worsens
■ symptoms persist for more than 7 days
■ symptoms clear up and occur again within a few days

Premature ejaculation may be due to a condition requiring medical supervision. If this product, used as directed, does not provide relief, discontinue use and consult a doctor.

Inactive ingredients

INACTIVE INGREDIENT SECTION

alcohol, citric acid, FD&C yellow no. 5, FD&C yellow no. 6, iodopropynyl butylcarbamate, methylisothiazolinone, nonylphenol ethoxylate, propylene glycol, water

Uses

INDICATIONS & USAGE SECTION

helps in temporarily slowing the onset of ejaculation

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Purpose

OTC - PURPOSE SECTION

Male Genital Desensitizer

label.jpg

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabellabel.jpeg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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9b4cf230-fd05-41d5-98c6-5db9ecb27b86Product name120230117
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625
7d755fa1-1087-4dcd-98f0-6d4bba479a57Product name320210602
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
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c08ab52f-2fc8-4409-9d9f-ed8edc0bd070Product name120171221
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
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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.

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87187-000187187-0001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
52469c23-ee90-88df-e063-6294a90a7f3d417bc541-df30-cb8a-e063-6294a90af49f2026-05-20WarningsExact identifier
spl set id: 417bc541-df30-cb8a-e063-6294a90af49f

Reported adverse events (FAERS/openFDA)#

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