WALGREENS ANTI ITCH CREAM- anti itch cream cream 
Walgreens Company

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.

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Walgreens Anti Itch Cream 

Drug Facts:

Active ingredients

Diphenhydramine hydrochloride 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

Inactive ingredients

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

(Purified) 

Other Information 

Principal Display Panel 1.0 oz Carton

Walgreens  NDC 0363-2315-28

Anti Itch Cream

Diphnhydramine HCL 2%    Topical analgesic 

Zinc Acetate 0.1%             Skin Protectant

NET WT 1.0  (28g)

Principal Display Panel 1.0 oz Carton

Principal Display Panel 1.0 oz Tube

Walgreens      NDC 0363-2315-28

Anti Itch Cream 

Diphenhydramine HCL 2.0%    Topical Analgesic 

Zinc Acetate 0.1%                  Skin Protectant

NET WT 1.0 oz (28g)

Principal Display Panel 1.0 oz Tube

WALGREENS ANTI ITCH CREAM 
anti itch cream cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-2315
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)  
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PEG-20 STEARATE (UNII: NBX892EA57)  
PROPYLENE GLYCOL MONOSTEARATE (UNII: MZM1I680W0)  
Propylene Glycol (UNII: 6DC9Q167V3)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-2315-281 in 1 CARTON05/05/2014
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 finalpart34705/05/2014
Labeler - Walgreens Company (008965063)

Revised: 11/2021
Document Id: 2495d04d-14be-4707-b3d3-a57e5f3845f3
Set id: b545553a-283a-48af-adc5-763758a9ff24
Version: 1
Effective Time: 20211101
 
Walgreens Company