EXTRA STRENGTH ITCH STOPPING- itch stopping cream cream 
Universal Distribution Centre LLC

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EXTRA STRENGTH ITCH STOPPING CREAM

Uses

Drug Facts

Active ingredientsPurpose
Diphenhydramine hydrochloride 2%Topical analgesic
Zinc acetate 0.1%Skin protectant

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 or does not improve within 7 days
  • 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

Inactive ingredients

cetyl alcohol, diazolidinyl urea, methylparaben, polyethylene glycol monostearate 1000, propylene glycol, propylparaben, purified water

Questions?

Call toll-free 1-800-222-1222

Distributed by:

Universal Distribution Centre LLC

96 Distribution Boulevard, Edison
NJ 08817

PRINCIPAL DISPLAY PANEL - 35.4 g Tube Carton

LabelEXTRA STRENGTH

Topical Analgesic/Skin Protectant

ITCH

STOPPING

CREAM

NET WT 1.25 OZ (35.4 g)

EXTRA STRENGTH  ITCH STOPPING
itch stopping cream cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52000-071
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
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
WATER (UNII: 059QF0KO0R)  
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52000-071-041 in 1 CARTON01/21/2021
1NDC:52000-071-0335.4 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01601/21/2021
Labeler - Universal Distribution Centre LLC (019180459)
Registrant - Savvy Care and Cosmetics Pvt. Ltd. (915039748)
Establishment
NameAddressID/FEIBusiness Operations
Savvy Care and Cosmetics Pvt. Ltd.915039748manufacture(52000-071)

Revised: 5/2024
Document Id: 1853be3d-62de-dc6b-e063-6394a90aad99
Set id: b9a42aa3-1903-76f0-e053-2a95a90a51d1
Version: 3
Effective Time: 20240513
 
Universal Distribution Centre LLC