ANTI-ITCH- diphenhydramine hydrochloride and zinc acetate cream 
Target Corporation

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Target Up &Up Anti-itch Cream

Drug Fact 

Active Ingredients

Diphenhydramine HCL 2%

Zinc Acetate 0.1%

Purpose

Topical analgesic 

Skin protectant 

Uses 

For temporary relief from pain and itching associated with :

Dries the oozing and weeping of poison

Warnings

For external use only

Do not use

Ask a Doctor before use

When using this product avoid contact with eyes.

Stop use and ask a doctor if

Keep this and all drugs out of the reach of children. If swallowed get medical help or contact a Poison Control Center immediately.

Directions 

Other information 

Store at controlled room temperature 20°-25°C (68° - 77°F)
Close the cap tightly after use

Inactive ingredients 

Cetyl Alcohol, Citric Acid, Diazolldinyl Urea, Glyceral Stearate, Methylparaben, Polyethylene Glycol Monsterate 1000, Sodium Citrate, Water

(Purified)

Questions or comments? 1-800-910-6874

Principal Display Panel 

Target Up&Up    NDC 11673-865-28

Extra Strength Itch Relief 

Diphenhydramine HCL 2% / Zinc Aceate 0.1%

Anti-itch cream

NET WT 1 OZ (28g)

290890 Tube

590890 Carton

ANTI-ITCH 
diphenhydramine hydrochloride and zinc acetate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-895
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 CATION1 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
CETYL ALCOHOL (UNII: 936JST6JCN)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
POLYETHYLENE GLYCOL 10000 (UNII: H57W405143)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11673-895-281 in 1 CARTON01/31/2024
128 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01701/31/2024
Labeler - Target Corporation (006961700)
Registrant - Sheffield Pharmaceuticals LLC (151177797)
Establishment
NameAddressID/FEIBusiness Operations
Sheffield Pharmaceuticals LLC151177797MANUFACTURE(11673-895) , analysis(11673-895)

Revised: 1/2024
Document Id: 8b820373-a3bd-42f2-aef3-3296d8227d73
Set id: f444b0a6-2ed3-4236-8206-342150290675
Version: 2
Effective Time: 20240117
 
Target Corporation