BENADRYL EXTRA STRENGTH ITCH STOPPING- diphenhydramine hydrochloride gel 
Johnson & Johnson Consumer Inc.

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Benadryl ® EXTRA STRENGTH ITCH STOPPING GEL

Drug Facts

Active ingredient

Diphenhydramine HCl 2%

Purpose

Topical Analgesic

Use

Warnings

For external use only.

Do not use

  • on large areas of the body
  • with any other product containing diphenhydramine, even one taken by mouth

Ask a doctor before use

  • on chicken pox
  • on measles

When using this product avoid contact with eyes

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

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

Directions

Other information

Store at Room Temperature

Inactive ingredients

SD alcohol 38-B, camphor, citric acid, diazolidinyl urea, glycerin, hydroxypropyl methylcellulose, methylparaben, propylene glycol, propylparaben, purified water, sodium citrate

Questions or comments?

call 1-877-717-2824 (toll free) or 215-273-8755 (collect) www.benadryl.com

Distributed by:
JOHNSON & JOHNSON
CONSUMER INC.

Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 103 mL Tube Label

Benadryl®

®

Cooling relief for

most outdoor itches

EXTRA STRENGTH

For Skin Use Only

ITCH STOPPING

GEL

Diphenhydramine HCl 2% /

Topical Analgesic

Insect

Bites
Poison Ivy,

Oak, Sumac
Mosquito

Bites
SunburnMinor Cuts

& Scrapes

3.5 FL OZ (103 mL)

Benadryl_01

BENADRYL EXTRA STRENGTH ITCH STOPPING 
diphenhydramine hydrochloride gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0242
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE20 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
GLYCERIN (UNII: PDC6A3C0OX)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
WATER (UNII: 059QF0KO0R)  
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0242-3103 mL in 1 TUBE; Type 0: Not a Combination Product10/01/2013
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01710/01/2013
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 1/2024
Document Id: 0f35912f-95e5-39f5-e063-6394a90a5f7b
Set id: 66a2fd60-1757-45cc-a195-ecb9241dca2a
Version: 6
Effective Time: 20240118
 
Johnson & Johnson Consumer Inc.