CAREALL ANTI-ITCH- diphenhydramine hydrochloride and zinc acetate cream cream 
New World Imports, Inc

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Active Ingredients

Diphenhydramine Hydrochloride 2%

Zinc Acetate 0.1%

Purpose

Diphenhydramine Hydrochloride 2%....Topical Analgesic

Zinc Acetate 0.1%.............................Skin Protectant

Keep out of Reach of Children

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

Uses

Uses

  • temporarily relieves pain and itching associated with: insect bites, minor burns, sunburn, minor skin irritations, minor cuts, scrapes, rashes due to poison ivy / poison oak / poison sumac.
  • dries the oozing and weeping of poison ivy, poison oak and poison sumac.

Warnings

For external use only.

Due 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 or does not improve within 7 days
  • symptoms persists for more than 7 days or clear up and occur again within a few days

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

cetyl alcohol, glyceryl monostearate, glycerin, methylparaben, propylparaben, carbopol 980, light liquid paraffin, polysorbate 60, stearic acid, purified water

AI125 Label

CAREALL ANTI-ITCH 
diphenhydramine hydrochloride and zinc acetate cream cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51824-088
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE20 mg  in 1 g
ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37) ZINC ACETATE1 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
Cetyl Alcohol (UNII: 936JST6JCN)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
GLYCERIN (UNII: PDC6A3C0OX)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
CARBOMER 980 (UNII: 4Q93RCW27E)  
PARAFFIN (UNII: I9O0E3H2ZE)  
POLYSORBATE 60 (UNII: CAL22UVI4M)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
WATER (UNII: 059QF0KO0R)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:51824-088-0135 g in 1 TUBE; Type 0: Not a Combination Product07/01/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01707/01/2022
Labeler - New World Imports, Inc (075372276)

Revised: 1/2024
 
New World Imports, Inc