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TN Dickinsons Pain and Itch Relief

Dosage form
LIQUID
Labeler
Dickinson Brands Inc.
Label updated
2026-02-05
Retrieved
2026-09-07
Active ingredients
PRAMOXINE HYDROCHLORIDE · ZINC ACETATE
View original label and images on DailyMed ↗
Label information

Drug Facts

유효 성분

성분·작용

Active ingredients Purposes
Pramoxine Hydrochloride (1.0%) Topical analgesic
Zinc Acetate (0.1%) Skin protectant
Uses

Temporarily relieves pain and itching associated with:

  • minor skin irritations
  • minor burns
  • sunburn
  • scrapes
  • minor cuts
  • insect bites
  • poison ivy, oak & sumac
    • Dries the oozing and weeping of poison ivy, oak & sumac
Warnings

For external use only

When using this product

  • do not get into eyes

Stop use and ask doctor if

  • condition or symptoms get worse or lasts more than 1 week
  • symptoms clear up and occur again within a few days

Do not use on

  • deep or puncture wounds
  • animal bites
  • serious burns

Label information

Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away.

Directions
  • apply to affected area not more than 3 to 4 times daily
  • children under 2 years of age: do not use, consult a doctor
Other information

protect from freezing

Inactive ingredients

aloe barbadensis leaf juice, benzoic acid, coco glucoside, witch hazel distillate, propanediol, tocopheryl acetate (vitamin E)

QUESTIONS OR COMMENTS?

TNDickinsons.com
1•888•860•2279

Label information

Dist. by: Dickinson Brands Inc.
East Hampton, CT 06424

PRINCIPAL DISPLAY PANEL - 103.5 mL Bottle Label

#1 PHYSICIAN RECOMMENDED*
WITCH HAZEL BRAND

CLEANSE • SOOTHE • RELIEVE

T.N.
DICKINSON'S®

Witch hazel®
+First Aid Pain Reliever & Skin Protectant

Pain & Itch Relief Foam

MAXIMUM STRENGTH

Soothes & Comforts
minor cuts, burns, irritation,
bug bites, poison ivy & rashes.

MADE WITH
100% NATURAL
WITCH HAZEL

APPLIES EASILY FROM HEAD TO TOE

3.5 FL. OZ. (103.5 mL)

[Image in the official label — see DailyMed source]

DailyMed Set ID: 537c9c27-ee81-4920-8e3f-21edb844c9cf · Version 2
NDC: 52651-056