EACH RELIEF EQUATE- diphenhydramine hci 2% gel 
Walmart

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active ingredient                              Purpose
Diphenhydramine HCI 2%................Topical analgesic

Uses Temporarily relieves pain due to: • minor burns • insect bites • sunburn • minor skin irritations • minor cuts • scrapes • rashes due to poison ivy, poison oak & poison sumac

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
When using this product • avoid contact with the eyes
Stop use and ask doctor if • condition gets worse • symptoms last more than 7 days • symptoms clear up and occur again in a few days.

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

Directions • do not use more than directed • adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily • children under 2 years of age: ask a doctor.

Inactive ingredients

Camphor, Citric Acid, Diazolidinyl
Urea, Glycerin, Hydroxypropyl Methylcellulose, Methylparaben,
Propylene Glycol, Propylparaben, SD Alcohol 38-B, Sodium
Citrate, Water.

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EACH RELIEF  EQUATE
diphenhydramine hci 2% gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49035-246
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE2 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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)  
ALCOHOL (UNII: 3K9958V90M)  
Sodium Citrate (UNII: 1Q73Q2JULR)  
Water (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49035-246-03103 mL in 1 TUBE; Type 0: Not a Combination Product04/03/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34804/03/2017
Labeler - Walmart (051957769)
Registrant - Product Quest Mfg (927768135)
Establishment
NameAddressID/FEIBusiness Operations
Product Quest Mfg927768135manufacture(49035-246) , label(49035-246)

Revised: 1/2017
Document Id: 4f32e6df-2272-40ef-b2d6-08af71dd5a05
Set id: 60e242bf-10e5-4627-a75d-b61c5302fbbb
Version: 1
Effective Time: 20170120
 
Walmart