Otc - Active Ingredient
Lidocaine 5% w/w
The following Structured Product Label (SPL) was submitted to the FDA by Weeks & Leo Compnay, Inc. for the product Oxify (NDC 11383-003). 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 otc - active ingredient, otc - ask doctor, otc - keep out of reach of children, otc - pregnancy or breast feeding, otc - purpose, otc - questions, otc - stop use, otc - when using, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Lidocaine 5% w/w
If swallowed, get medical help or contact a Poison Control Center right away.
Ask a health professional before use.
Local anesthetic
Call 833-358-6431
For External use only
Store at 25°C (77°F); excursions permitted to 15-30°C (59-86°F) [see USP Controoled Room Temperature]
Helps relieve the pain, itching, and burning associated with hemorrhoids and other anorectal disorders
Allergy alert: certain persons can develop allergic reactions to ingredients in this product.
acrylates/C10-30 alkyl acrylate crosspolymer, aloe barbadensis (aloe vera) leaf juice, aminomethyl propanol, C30-45 alkyl cetearyl dimethicone crosspolymer, caprylyl methicone, cetearyl alcohol, ceteth-20 phosphate, dicetyl phosphate, dimethicone, edetate
Changed Administration section to dosage and administration section
Oxify
Lidocaine 5% Anorectal (Hemorrhoidal) Cream
Relieves Pain
Relieves Itch
Relieves Burning
Net Wt. 6 oz (170 g)
* Please review the disclaimer below.