Label: RITE AID MAXIMUM STRENGTH PAIN RELIEVING- benzalkonium chloride and lidocaine hydrochloride liquid
- NDC Code(s): 11822-7220-5
- Packager: RITE AID
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Updated September 23, 2022
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- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
For external use only
When using this product
- do not use in or near the eyes
- do not apply over large areas of the body or in large quantities
- do not apply over raw surfaces or blistered areas
Stop use and ask a doctor if
- condition worsens
- symptoms persist for more than 7 days, or clear up and occur again within a few days
- Other information
- Inactive ingredients
Principal Display Package Label Panel
Compare to the active ingredients in Bectine® Max*
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.
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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
If you’re not satisfied we’ll happily refund your money.
INGREDIENTS AND APPEARANCE
RITE AID MAXIMUM STRENGTH PAIN RELIEVING
benzalkonium chloride and lidocaine hydrochloride liquid
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-7220 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g in 100 mL LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 4 g in 100 mL Inactive Ingredients Ingredient Name Strength EDETATE DISODIUM (UNII: 7FLD91C86K) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11822-7220-5 148 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/23/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 01/23/2020 Labeler - RITE AID (014578892)