TYLENOL PRECISE WARMING PAIN RELIEVING- lidocaine cream 
Johnson & Johnson Consumer Inc.

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Tylenol Precise Warming Pain Relieving Cream

Drug Facts

Lidocaine 4%

Topical analgesic

Uses

For the temporary relief of pain

Warnings

For external use only.

Do not use

  • in large quantities, particularly over raw surfaces or blistered areas

When using this product

  • avoid contact with eyes

Stop use and ask a doctor if

  • condition worsens or symptoms persist for more than 7 days
  • symptoms clear up and occur again within a few days

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other Information

store at 15 0 to 30 0 C (59 0 to 86 0 F)

Inactive Ingredients

carbomer copolymer, cetearyl olivate, cetyl alcohol, fragrance, glycerin, isopropyl palmitate, phenoxyethanol, sodium polyacrylate, sorbitan olivate, vanillyl butyl ether, water

Questions?

Call 1-877-895-3665 (toll-free) or 215- 273-8755 (collect)

Distributed by:

JOHNSON & JOHNSON CONSUMER INC.

Skillman, NJ 08558 USA

PRINCIPAL DISPLAY PANEL - 113 g Tube Carton

Warming

Pain Relieving Cream

Lidocaine 4%

TYLENOL ®

PRECISE TM

Fast acting

Targeted

penetrating

pain relief

ROLLER BALL

APPLICATOR

Maximum Strength Lidocaine

without a prescription

LIGHTLY SCENTED

For external

use only

NET WT 4.0 OZ (113 g)

Tylenol_01

TYLENOL PRECISE WARMING PAIN RELIEVING 
lidocaine cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0794
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE40 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
CETEARYL OLIVATE (UNII: 58B69Q84JO)  
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
VANILLYL BUTYL ETHER (UNII: S2ULN37C9R)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)  
SORBITAN OLIVATE (UNII: MDL271E3GR)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0794-41 in 1 CARTON02/12/2024
1113 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01702/12/2024
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 12/2023
Document Id: 0c60c97c-f670-569c-e063-6394a90a180d
Set id: 0c60b607-ade9-68f2-e063-6394a90a4025
Version: 1
Effective Time: 20231213
 
Johnson & Johnson Consumer Inc.