Other
Drug Facts
DISTRIBUTED BY:
Target Corporation.,
Minneapolis, MN 55403
The following Structured Product Label (SPL) was submitted to the FDA by Target Corporation for the product Jock Itch Cream (NDC 11673-436). 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 other, otc - active ingredient, otc - purpose, uses, warnings, do not use, otc - when using, otc - stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Drug Facts
DISTRIBUTED BY:
Target Corporation.,
Minneapolis, MN 55403
Butenafine Hydrochloride 1%
Antifungal
For external use only
When using this product do not get into the eyes. If eye contact occurs, rinse thoroughly with water.
Stop use and ask a doctor if too much irritation occurs or irration gets worse.
Keep out of reach of children. If swallowed, get medical help or contact a Poision Control Center right away.
Benzyl Alcohol, Cetyl Alcohol, Glycerin, Glyceryl Monostearate SE, Polyoxyethylene (23) Cetyl Ether, Propylene Glycol Dicaprylate, Purified Water, Sodium Benzoate, Stearic Acid, Trolamine, White Petrolatum.
1-800-910-6874
Compare to active ingredient in Lotrimin Ultra ® Jock Itch*
Jock Itch
Cream
Butenafine Hydrochloride
Cream 1%
butenafine hydrochloride
up&up TM
NET WT 0.42 oz (12 g)
* Please review the disclaimer below.