ANTI-ITCH- diphenhydramine hydrochloride and zinc acetate cream

Anti-itch by

Drug Labeling and Warnings

Anti-itch by is a Otc medication manufactured, distributed, or labeled by Target Corporation, Sheffield Pharmaceuticals LLC, Sheffield Pharmaceuticals LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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 :

• insect bites
• minor burns
• sunburn
• minor skin irritations
• rashes due to poison ivy, poison oak, and poison sumac

Dries the oozing and weeping of poison

• ivy
• oak
• 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 the 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

• conditions worsen or does not improve within 7 days
• symptoms persist for more than 7 days or clear up and occur agian within a few days

KEEP OUT OF REACH OF CHILDREN

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

Directions 

• do not use more than directed
• adults and children 2 years of age and older; apply to affected areas not more than 3 to 4 times daily
• children under 2 years of age , consult a doctor

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)

INGREDIENTS AND APPEARANCE

ANTI-ITCH 
diphenhydramine hydrochloride and zinc acetate cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11673-895
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M)	DIPHENHYDRAMINE HYDROCHLORIDE	20 mg  in 1 g
ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	1 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11673-895-28	1 in 1 CARTON	01/31/2024
1		28 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	01/31/2024

Labeler - Target Corporation (006961700)

Registrant - Sheffield Pharmaceuticals LLC (151177797)

Establishment
Name	Address	ID/FEI	Business Operations
Sheffield Pharmaceuticals LLC		151177797	MANUFACTURE(11673-895) , analysis(11673-895)