Rite Aid Maximum Strength Liquid
FDA Label NDC 11822-7220

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Rite Aid for the product Rite Aid Maximum Strength (NDC 11822-7220). 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 - purpose, uses, warnings, ask a doctor before use if you have, when using this product, stop use and ask a doctor if, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Principal Display Package Label Panel

Compare to the active ingredients in Bectine® Max*

NDC# 11822-7220-5

MAXIMUM STRENGTH

pain relieving

ANTISEPTIC SPRAY

NO STING

FIRST AID ANTISEPTIC & PAIN RELIEVER

Kills 99% of Germs*

MAX STRENGTH GERM KILLING

4% Lidocaine HCl

MAX STRENGTH PAIN RELIEVER

*Germs commonly associated with skin infection.

To unlock, push in tab and twist right.

To lock, twist left until locked

5 FL OZ (148 mL)

*This product is not manufactured or distributed by WellSpring Pharmaceuticals Corporation, owner of the registered trademark Bectine® Max.

DISTRIBUTED BY: RITEAID, 30 HUNTER LANE,

CAMP HILL, PA 17011

www.riteaid.com

SATISFACTION GUARANTEE:

If you’re not satisfied we’ll happily refund your money.

* Please review the disclaimer below.