Zinc Oxide Ointment 20%

Manufacturer
Aldermed Inc.
Effective date
2026-05-04
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:56:22

Label at a glance#

ProductZinc Oxide Skin Protectant
Active ingredientZINC OXIDE
Label structure9 sections

Indications and uses

• Dries the oozing and weeping of poison: • Ivy • Oak • Sumac

Dosage and administration

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

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide USP 20% w/w

Purpose

OTC - PURPOSE SECTION

Skin Protectant

Uses

INDICATIONS & USAGE SECTION

• Dries the oozing and weeping of poison: • Ivy • Oak • Sumac

Warnings

WARNINGS SECTION

For External Use Only

When using this product

OTC - WHEN USING SECTION

• Do not get into eyes

• Do not use over large areas of the body

Stop use and ask a doctor if

OTC - STOP USE SECTION

• 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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

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

Other Information

OTHER SAFETY 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

INACTIVE INGREDIENT SECTION

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

Questions?

OTC - QUESTIONS SECTION

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

Tube and carton 30 g

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabelboxbox

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
198911zinc oxide 20 % Topical OintmentPSN5
198911zinc oxide 0.2 MG/MG Topical OintmentSCD5
198911zinc oxide 20 % Topical OintmentSY5
198911zinc oxide 200 MG per GM Topical OintmentSY5
198911ZNO 0.2 MG/MG Topical OintmentSY5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87236-007-01Zinc OxideSkin Protectant1 in 1 CARTONOINTMENT15
87236-007-01Zinc OxideSkin Protectant30 g in 1 TUBEOINTMENT305
87236-007-16Zinc OxideSkin Protectant454 g in 1 JAROINTMENT4545
87236-007-28Zinc OxideSkin Protectant1 in 1 CARTONOINTMENT15
87236-007-28Zinc OxideSkin Protectant28.4 g in 1 TUBEOINTMENT28.45
87236-007-56Zinc OxideSkin Protectant56.6 g in 1 TUBEOINTMENT56.65
87236-007-56Zinc OxideSkin Protectant1 in 1 CARTONOINTMENT15

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87236-00787236-007-01, 87236-007-28, 87236-007-56, 87236-007-16

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
42026-02-12monthly-update2026-06-03 17:56:29
22026-01-23monthly-update2026-06-03 17:53:10
12025-12-09monthly-update2026-06-03 17:45:39

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Zinc Oxide Skin ProtectantZINC OXIDE 20%Aldermed Inc.a55ac5b4-bac7-4d2a-8ac8-c3eaf7e89e522026-05-04WarningsExact identifier
ndc (package): 87236-007-16
ndc (package): 87236-007-28
ndc (package): 87236-007-01
ndc (package): 87236-007-56
ndc (product): 87236-007
ndc11 (package): 87236000716
ndc11 (package): 87236000728
ndc11 (package): 87236000756
ndc11 (package): 87236000701
spl id: 5101e1fe-dffa-1e92-e063-6394a90ae61f
spl set id: a55ac5b4-bac7-4d2a-8ac8-c3eaf7e89e52

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.