The following Structured Product Label (SPL) was submitted to the FDA by Cjh Innovations Llc for the product Maxgro (NDC 87187-0001). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding dosage & administration, warnings, inactive ingredients, uses, keep out of reach of children, purpose, label.jpg, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
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.
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.
alcohol, citric acid, FD&C yellow no. 5, FD&C yellow no. 6, iodopropynyl butylcarbamate, methylisothiazolinone, nonylphenol ethoxylate, propylene glycol, water
helps in temporarily slowing the onset of ejaculation
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Male Genital Desensitizer
Label (Label)
* Please review the disclaimer below.
