ROLL-ON PAIN RELIEF LIQUID- lidocaine hcl gel

Roll-On Pain Relief Liquid by

Drug Labeling and Warnings

Roll-On Pain Relief Liquid by is a Otc medication manufactured, distributed, or labeled by HyVee Inc, Nantong Health & Beyond Hygienic Products Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Lidocaine HCl 4%

Purpose

Topical Analgesic

Use

Temporarily relieves minor pain

Warnings

For External use only

Do not use

Do not use

■on large areas of the body or on cut, irritated or swollen skin
■on puncture wounds

■for more than one week without consulting a doctor

When using this product

When using this product

■use only as directed. Read and follow all directions and warnings on this carton

■do not allow contact with the eyes and mucous membranes

■do not bandage or apply local heat (such as heating pads) or a medicated patch to area of use

■do not use at the same time as other topical analgesics

Stop use and ask a doctor if

Stop use and ask a doctor if

■condition worsens

■ redness is present
■irritation develops

■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.

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 children 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 information

Store at room temperature

Inactive Ingredients

Inactive ingredients acrylates/C10-30 alkyl acrylate crosspolymer (60000 MPA.S), aloe barbadensis leaf juice, am nomethylpropanol, ceteth-10 phosphate, cetostearyl alcohol, cyclomethicone 5, dicetyl phosphate, dimethicone 350, dimethicone/vinyl dimethicone
crosspolymer (soft particle), disodium EDTA, ethylhexylglycerin, glyceryl 1 stearate, hydroxyethyl acrylate/sodium acryloyld methyl taurate copolymer (100000 MPA.S at 1.5%), sohexadecane, phenoxyethanol, SD alcohol, steareth-21, water

Questions or comments?

Call 1-866-326-1313

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ROLL-ON PAIN RELIEF LIQUID 
lidocaine hcl gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 42507-916
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
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
DIMETHICONE 350 (UNII: 2Y53S6ATLU)
WATER (UNII: 059QF0KO0R)
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
CETETH-10 PHOSPHATE (UNII: 4E05O5N49G)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
STEARETH-21 (UNII: 53J3F32P58)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ISOHEXADECANE (UNII: 918X1OUF1E)
GLYCERYL 1-STEARATE (UNII: 258491E1RZ)
ALCOHOL (UNII: 3K9958V90M)
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)
DICETYL PHOSPHATE (UNII: 2V6E5WN99N)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 42507-916-01	73 g in 1 BOTTLE; Type 0: Not a Combination Product	03/01/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	03/01/2026

Labeler - HyVee Inc (006925671)

Establishment
Name	Address	ID/FEI	Business Operations
Nantong Health & Beyond Hygienic Products Inc.		421280161	manufacture(42507-916)