Skip to Content

Each Relief Equate

Medically reviewed on Jan 20, 2017

Dosage form: gel
Ingredients: DIPHENHYDRAMINE HYDROCHLORIDE 2g in 100mL
Labeler: Walmart
NDC Code: 49035-246

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.

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.

EACH RELIEF  EQUATE
diphenhydramine hci 2% gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49035-246
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIPHENHYDRAMINE HYDROCHLORIDE (DIPHENHYDRAMINE) DIPHENHYDRAMINE HYDROCHLORIDE2 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
CAMPHOR (SYNTHETIC) 
CITRIC ACID MONOHYDRATE 
Diazolidinyl Urea 
Glycerin 
HYPROMELLOSE, UNSPECIFIED 
Methylparaben 
Propylene Glycol 
Propylparaben 
ALCOHOL 
Sodium Citrate 
Water 
Packaging
#Item CodePackage Description
1NDC:49035-246-03103 mL in 1 TUBE
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/FEIOperations
Product Quest Mfg927768135manufacture(49035-246), label(49035-246)

 
Walmart

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Hide