PAIN RELIEF LIDOCAINE- lidocaine cream

Pain Relief Lidocaine by

Drug Labeling and Warnings

Pain Relief Lidocaine by is a Otc medication manufactured, distributed, or labeled by Kroger Company, Nantong Health & Beyond Hygienic Products Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Lidocaine HCl 4%

Purpose

Topical anesthetic

Uses

Temporarily relieves minor pain

Warnings

For external use only. Avoid contact with eyes.

Do not use

• on a large areas of the body or on cut, irritated or swollen skin
• on punture wounds
• for more than one week without consulting a doctor

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

If pregnant or breast feeding,

ask a health professional before use

Keep out of reach of children and pets

If swallowed, get medical help or contact Poison Control Center (1-800-222-1222) right away.

Directions

• adults and childrens over 12 years: apply a thin layer to affected area every 6 to 8 hours, not to exceed 3 applications in a 24 hour period.
• Children 12 years or younger: ask a doctor

Other

Store at room temperature

Inactive Ingredients

alcohol, aloe vera leaf, aminomethylpropanol, carbomer interpolymer type A, cyclomethicone 5, dihexadeycl phosphete, dimeticone, dimeticone/vinyl dimeticone crosspolymer, edetate disosium, ethylhexylglycerin, glyceryl 1 stearate, hydroxyethyl acrylate/sodium acryloyldimethyl taurate copolymer, isohexadecane, phenoxyethanol, steareth-21, water.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PAIN RELIEF LIDOCAINE 
lidocaine cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 41226-695
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	4 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
ISOHEXADECANE (UNII: 918X1OUF1E)
DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N)
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
WATER (UNII: 059QF0KO0R)
DIMETHICONE (UNII: 92RU3N3Y1O)
GLYCERYL 1-STEARATE (UNII: 258491E1RZ)
ALCOHOL (UNII: 3K9958V90M)
STEARETH-21 (UNII: 53J3F32P58)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 41226-695-01	76.5 g in 1 TUBE; Type 0: Not a Combination Product	02/01/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	02/01/2026

Labeler - Kroger Company (006999528)

Establishment
Name	Address	ID/FEI	Business Operations
Nantong Health & Beyond Hygienic Products Inc.		421280161	manufacture(41226-695)