ICEQUAKE LIDOCAINE ANALGESIC- lidocaine hydrochloride liquid 
Southern Sales & Service, Inc.

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IceQuake Lidocaine Analgesic

Drug Facts

Active ingredient

Lidocine HCl 4%

Purpose

Topical anesthetic

Use

Temporarily relieves minor pain

Warnings

For external use only

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

  • use only as directed. Read and follow all directions and warnings on this label.
  • do not allow contact with the eyes
  • do not bandage or apply local heat (such as heating pads) to area of use

Do not use

condition worsens Stop use and ask a doctor if

Flammable

keep away from fire or flame

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 a Poison Control Center right away.

Directions

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

Inactive ingredients

Disodium EDTA, isopropyl alcohol, glycerin, methylparaben, polysorbate 20, propylparaben, purified water, xanthan gum.

IceQuake Lidocaine Topical Analgesic Liquid 74ml

front labelfacts panel

ICEQUAKE LIDOCAINE ANALGESIC 
lidocaine hydrochloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69822-430
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS4 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
GLYCERIN (UNII: PDC6A3C0OX)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
WATER (UNII: 059QF0KO0R)  
XANTHAN GUM (UNII: TTV12P4NEE)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69822-430-0374 mL in 1 BOTTLE; Type 0: Not a Combination Product08/01/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01708/01/2022
Labeler - Southern Sales & Service, Inc. (013114906)
Registrant - Southern Sales & Service, Inc. (013114906)

Revised: 11/2023
Document Id: 0b57eb9f-300d-283f-e063-6394a90a2f97
Set id: 9089cb78-e9f8-4437-a767-df809a114c4b
Version: 2
Effective Time: 20231129
 
Southern Sales & Service, Inc.