HIMS DELAY WIPES- benzocaine wipes dressing

Hims Delay Wipes by

Drug Labeling and Warnings

Hims Delay Wipes by is a Otc medication manufactured, distributed, or labeled by Hims Inc., Swiss-American CDMO, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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.

Indications

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

INGREDIENTS AND APPEARANCE

HIMS DELAY WIPES 
benzocaine wipes dressing

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71730-009
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	70 g  in 1000 g

Inactive Ingredients
Ingredient Name	Strength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71730-009-03	3 in 1 CARTON	06/14/2021
1		3 g in 1 POUCH; Type 0: Not a Combination Product
2	NDC: 71730-009-12	12 in 1 CARTON	06/14/2021
2		3 g in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	06/14/2021

Labeler - Hims Inc. (080678637)

Registrant - Swiss-American CDMO, LLC (080170933)

Establishment
Name	Address	ID/FEI	Business Operations
Swiss-American CDMO, LLC		080170933	manufacture(71730-009)