Hims Delay Wipes Dressing
FDA Label NDC 71730-009

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Hims Inc. for the product Hims Delay Wipes (NDC 71730-009). 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 warnings, directions, indications, active ingredient, inactive ingredient, keep out of reach of children, quesitons?, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Warnings

For external use only

When using this prouct avoid contact with the eyes


Stop and ask doctor if: the product, used as directed, does not provide relief.  Premature ejaculation may be due to a condition requiring medical supervision. You or your partner develop a rash or irritation, such as burning or itching. If symptoms persist.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Apply a small amount to head and shaft of penis before intercourse, or use as directed by a doctor. Wash product off after intercourse.

Indications

For reducing oversensitivity in the male in advance of intercourse.

For reducing oversensitivity in the male in advance of intercourse.

Active Ingredient

Benzocaine 7% Male Genital Desensitizer

Inactive Ingredient

Propylene glycol

Keep Out Of Reach Of Children

Keep out of reach of children

Quesitons?

For questions or comments call 1-800-368-0038   

Other Information

Made in the USA with US and imported materials.

Distributed by HIMS, Inc., 2269 Chestnut Street #523, San Francisco, CA 94123

Labeling

* Please review the disclaimer below.