Medicine guide

Diphenhydramine Hydrochloride and Zinc Acetate

20 mg/g + 1 mg/g · Cream

  • Available without prescription
  • Copper Absorption Inhibitor
Made by
STRATEGIC SOURCING SERVICES LLC

Quoted from the official source. Not yet reviewed by Mediclarum — the leaflet in your pack is authoritative.

At a glance

Quoted from the official label · 2026-03-03

What it is

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

Used for
  • Insect bites minor burns sunburn minor skin irritations minor cuts scrapes rashes due to poison ivy, poison oak, and poison sumac dries the oozing and weeping of poison ivy, poison oak, and poison sumac
Do not take it if

On large areas of the body with any other product containing diphenhydramine, even one taken by mouth

All warnings ↓
Good to know
  • Sold without a prescription
  • FDA enforcement reports list no ongoing recall, and none from the last two years, for this product code · checked 2026-10-02
15other products contain Diphenhydramine Hydrochloride and Zinc Acetate — compare makers, forms and strengths

Every line above is selected, not written, from the official label. Nothing is reworded. DailyMed

What it is for

temporarily relieves pain and itching associated with:

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

From the official label · 2026-03-03 · DailyMed

Do not take it if

on large areas of the body with any other product containing diphenhydramine, even one taken by mouth

Quoted from the official label, section “OTC — Do Not Use”.

How to take it

These directions are for this exact strength and form. Another one is different.

  • 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

Quoted from the official label, section “Dosage & Administration”.

Ask a doctor first if

on chicken pox on measles

Quoted from the official label, section “OTC — Ask Doctor”.

Stop and get help 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

Quoted from the official label, section “OTC — Stop Use”.

Other 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.
  • avoid contact with eyes

Quoted from the official label, section “Warnings”.

Keep away from children

If swallowed, get medical help or contact a Poison Control Center right away.

Quoted from the official label, section “OTC — Keep Out of Reach of Children”.

How to store it

  • to open:
  • unscrew cap, use pointed end of cap to puncture seal.
  • store at 20° to 25°C (68° to 77°F) see carton or tube crimp for lot number and expiration date

Quoted from the official label, section “Storage and Handling”.

What kind of medicine it is

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

Quoted from the official label, section “OTC — Purpose”.

Other ingredients

Relevant if you react to a dye, a preservative, lactose or gluten.

cetyl alcohol, glyceryl stearate, glyceryl stearate/PEG-100 stearate, methylparaben, propylene glycol, propylparaben and purified water

Quoted from the official label, section “Inactive Ingredients”.

Questions about this product

call 833-358-6431 Monday to Friday 9:00am to 7:00pm EST

Quoted from the official label, section “OTC — Questions”.

Ingredients people check for

Lactose, gluten, dyes, sugars and other ingredients that matter with an allergy, intolerance or diet — as this product’s FDA label lists them.

Same active substance, strength and form in other countries

Matched on active substance, strength and kind of form only. This is not a statement that the products are equivalent or interchangeable: other ingredients, release and approved uses can differ — ask a pharmacist before swapping.

Medicine passport: one printable page to show a pharmacist abroad

CanadaNo exact match for this strength and form

Details

Made bySTRATEGIC SOURCING SERVICES LLC
Active substanceDiphenhydramine Hydrochloride and Zinc Acetate
Used inBreathing, airways, allergies and cough
Strength20 mg/g + 1 mg/g
FormCream
RouteTopical
Packs1 TUBE in 1 CARTON / 28.4 g in 1 TUBE
NDC70677-1213

Source: NDC Directory · 2026-09-13 · not reviewed by a clinician

Source: US Food and Drug Administration, NDC Directory. Reuse terms: US government work (FDA).

Other strengths and forms

2 products are sold under this name. Grouped by form; a number on a strength means several companies make it.

Same active substance

These contain the same substance. That does not mean one can replace another — ask a pharmacist.