ZINC OXIDE SKIN PROTECTANT- zinc oxide 20% ointment

Zinc Oxide by

Drug Labeling and Warnings

Zinc Oxide by is a Otc medication manufactured, distributed, or labeled by Aldermed Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Zinc Oxide USP 20% w/w

Purpose

Skin Protectant

Uses

Dries the oozing and weeping of poison: Ivy Oak Sumac

Warnings

For External Use Only

When using this product

Do not get into eyes

Do not use over large areas of the body

Stop use and ask a doctor if

The condition worsens

Symptoms last more than 7 days or clear up and occur again within a few days

You are allergic to any of these ingredients

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

Directions

For poison ivy, oak, and sumac: apply as needed.

Other Information

To open, unscrew cap, pull tab to remove foil seal.

• Store at 20 to 25 C (68 to 77 F)
  • Preserve in well-closed container.
  • See carton ot ube crimp for Lot number and expiration date.

Inactive Ingredients

Cetostearyl Alcohol, Light Mineral Oil, Macrogol Cetostearyl Ether 20, White Petrolatum.

Questions?

Call 1-833-605-84-74 9am-5 pm EST M-F

Tube and carton 30 g

INGREDIENTS AND APPEARANCE

ZINC OXIDE  SKIN PROTECTANT
zinc oxide 20% ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87236-007
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	20 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
LIGHT MINERAL OIL (UNII: N6K5787QVP)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
WHITE PETROLATUM (UNII: B6E5W8RQJ4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87236-007-01	1 in 1 CARTON	12/01/2025	01/01/2026
1		30 g in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 87236-007-28	1 in 1 CARTON	12/01/2025
2		28.4 g in 1 TUBE; Type 0: Not a Combination Product
3	NDC: 87236-007-56	1 in 1 CARTON	12/01/2025
3		56.6 g in 1 TUBE; Type 0: Not a Combination Product
4	NDC: 87236-007-16	454 g in 1 JAR; Type 0: Not a Combination Product	12/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	12/01/2025

Labeler - Aldermed Inc. (144887712)