allergy cream with zinc acetate

allergy cream with zinc acetate
SPL v1
SPL
SPL Set ID 9575213f-64ca-47ac-b2bd-01f973af910b
Route
topical
Published
Effective Date 2014-03-27
Document Type 34390-5 HUMAN OTC DRUG LABEL

Drug Facts

Composition & Product

Active Ingredients
diphenhydramine (2 mg) zinc cation (0.1 mg)
Inactive Ingredients
carbomer 940 cetyl alcohol glycerin glyceryl monostearate paraffin methylparaben polysorbate 60 propylparaben water stearic acid

Identifiers & Packaging

Marketing Status
otc monograph not final active Since 2014-03-27
Purpose

Topical analgesic Skin protectant

Description

Diphenhydramine hydrochloride, USP 2% Zinc acetate, USP 0.1%

Medication Information

Warnings

For external use only

Uses

For the temporary relief of pain and itching associated with

  • minor burns
  • sunburn
  • minor cuts
  • scrapes
  • insect bites
  • minor skin irritations
  • rashes due to poison ivy, oak and sumac
  • dries the oozing and weeping of poison:
    • ivy
    • oak
    • sumac
Purpose

Topical analgesic

Skin protectant

Directions
  • do not use more often 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
Other Information
  • Store between 59°-86°F (15°-30°C).
Description

Diphenhydramine hydrochloride, USP 2% Zinc acetate, USP 0.1%

Do Not Use
  • on large areas of the body
  • with any other product containing diphenhydramine, even one taken by mouth
Active Ingredient

Diphenhydramine hydrochloride, USP 2%

Zinc acetate, USP 0.1%

Inactive Ingredient

cetyl alcohol, methylparaben, polysorbate 60, propylene glycol, purified water, sorbitan monostearate

Ask A Doctor Before Use
  • on chicken pox
  • on measles
When Using This Product
  • avoid contact with the eyes
Stop Use and Ask A Doctor If
  • condition gets worse
  • 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.

Package Label.principal Display Panel

NDC 0363-0525-56

Walgreens  The Brand America Trusts®

Compare to the active ingredients in BENADRYL ® EXTRA STRENGTH ITCH STOPPING CREAM *

Wal-dryl

Topical Analgesic/Skin Protectant

ITCH RELIEF

MAXIMUM STRENGTH

2% Diphenhydramine Hydrochloride, USP and 0.1% Zinc Acetate, USP

Temporary Relief of Itch and Pain due to

• Insect Bites • Minor Skin Irritations •Rashes from Poison Ivy, Poison Oak or Poison Sumac

PHARMACIST RECOMMENDED

NET WT. 1 OZ (28 g)

05250111F1  VC110348

*This product is not affiliated with, manufactured by, or produced by the makers or owners of Benadryl®.

Made in USA

Distributed by: Walgreen Co.,

200 Wilmot Rd., Deerfield, IL 60015-4616

Quality Guaranteed

100% Satisfaction Guaranteed with all Walgreens Products or Your Money Back. www.walgreeens.com

Structured Label Content

Warnings (WARNINGS)

For external use only

Uses (USES)

For the temporary relief of pain and itching associated with

  • minor burns
  • sunburn
  • minor cuts
  • scrapes
  • insect bites
  • minor skin irritations
  • rashes due to poison ivy, oak and sumac
  • dries the oozing and weeping of poison:
    • ivy
    • oak
    • sumac
Purpose (PURPOSE)

Topical analgesic

Skin protectant

Directions (DIRECTIONS)
  • do not use more often 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
Other Information (OTHER INFORMATION)
  • Store between 59°-86°F (15°-30°C).
Do Not Use (DO NOT USE)
  • on large areas of the body
  • with any other product containing diphenhydramine, even one taken by mouth
Active Ingredient (ACTIVE INGREDIENT)

Diphenhydramine hydrochloride, USP 2%

Zinc acetate, USP 0.1%

Inactive Ingredient (INACTIVE INGREDIENT)

cetyl alcohol, methylparaben, polysorbate 60, propylene glycol, purified water, sorbitan monostearate

Ask A Doctor Before Use (ASK A DOCTOR BEFORE USE)
  • on chicken pox
  • on measles
When Using This Product (WHEN USING THIS PRODUCT)
  • avoid contact with the eyes
Stop Use and Ask A Doctor If (STOP USE AND ASK A DOCTOR IF)
  • condition gets worse
  • symptoms persist for more than 7 days or clear up and occur again within a few days
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.

Package Label.principal Display Panel (PACKAGE LABEL.PRINCIPAL DISPLAY PANEL)

NDC 0363-0525-56

Walgreens  The Brand America Trusts®

Compare to the active ingredients in BENADRYL ® EXTRA STRENGTH ITCH STOPPING CREAM *

Wal-dryl

Topical Analgesic/Skin Protectant

ITCH RELIEF

MAXIMUM STRENGTH

2% Diphenhydramine Hydrochloride, USP and 0.1% Zinc Acetate, USP

Temporary Relief of Itch and Pain due to

• Insect Bites • Minor Skin Irritations •Rashes from Poison Ivy, Poison Oak or Poison Sumac

PHARMACIST RECOMMENDED

NET WT. 1 OZ (28 g)

05250111F1  VC110348

*This product is not affiliated with, manufactured by, or produced by the makers or owners of Benadryl®.

Made in USA

Distributed by: Walgreen Co.,

200 Wilmot Rd., Deerfield, IL 60015-4616

Quality Guaranteed

100% Satisfaction Guaranteed with all Walgreens Products or Your Money Back. www.walgreeens.com

Advanced Ingredient Data

Raw Label Data

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Additional Information

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Source: dailymed · Ingested: 2026-02-15T11:55:46.410933 · Updated: 2026-03-14T22:53:43.600487