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
Drug Label Information
Updated November 11, 2023
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- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- Uses
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Warnings
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
- Directions
- Other information
- Inactive ingredients
- Questions?
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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.
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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
SATISFACTION GUARANTEE:
If you’re not satisfied we’ll happily refund your money.
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INGREDIENTS AND APPEARANCE
RITE AID MAXIMUM STRENGTH PAIN RELIEVING
benzalkonium chloride and lidocaine hydrochloride liquidProduct 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 Drug M003 01/23/2020 Labeler - RITE AID (014578892)