Zinc Oxide with Menthol & White Petrolatum

Manufacturer
Aldermed Inc.
Effective date
2026-05-04
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:56:28

Label at a glance#

ProductZinc Oxide with Menthol and White Petrolatum
Active ingredientMENTHOL, ZINC OXIDE, WHITE PETROLATUM
Label structure9 sections

Indications and uses

■ gives temporary relief of local itching and discomfort in the perianal area ■ temporarily forms a protective coating over inflamed tissues to help prevent drying of tissues ■ temporarily protects irritated areas  ■ temporarily relieves burning ■ provides temporary relief from skin irritations ■ temporarily protects the inflamed, irritated anorectal surface to help make bowel movements less painful ■ temporarily ...

Dosage and administration

■ Adults: when practical cleanse the affected area with mild soap and warm water and rinse thoroughly. Gently dry by patting or blotting with toilet tissue or a soft cloth before application of this product. Apply to affected area up to 6 times daily. ■ Children under 12 years of age: consult a doctor

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 0.44%

Zinc Oxide 20.625%

White Petrolatum USP 66.625%

Purpose

OTC - PURPOSE SECTION

Analgesic

External Analgesic

Astringent/Protectant

Uses

INDICATIONS & USAGE SECTION

■ gives temporary relief of local itching and discomfort in the perianal area

■ temporarily forms a protective coating over inflamed tissues to help prevent drying of tissues

■ temporarily protects irritated areas 

■ temporarily relieves burning

■ provides temporary relief from skin irritations

■ temporarily protects the inflamed, irritated anorectal surface to help make bowel movements less painful

■ temporarily protects inflamed perianal skin

■ temporarily relieves the symptoms of perianal skin irritation

■ may provide a cooling sensation

Warnings

WARNINGS SECTION

For external use only

Allergy Alert: certain persons can develop allergic reactions to ingredients in this product. If the symptom being treated does not subside or if redness, irritation, swelling, pain, or other symptoms develop or increase, discontinue use and consult a doctor.

When using this product

OTC - WHEN USING SECTION

■ do not exceed the recommended daily dosage unless directed by a doctor
■ do not put this product into the rectum by using fingers or any mechanical device or applicator

Stop use and ask a doctor if

OTC - STOP USE SECTION

■ condition worsens or does not improve in 7 days
■ bleeding occurs, consult a doctor promptly

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

■ Adults: when practical cleanse the affected area with mild soap and warm water and rinse thoroughly. Gently dry by patting or blotting with toilet tissue or a soft cloth before application of this product. Apply to affected area up to 6 times daily.


■ Children under 12 years of age: consult a doctor

Other Information

OTHER SAFETY INFORMATION

• Store at room temperature 15º-30º C (59º-86º F)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Calamine, Glycerine, Lanolin, Mineral Oil, Phenol, Sodium Bicarbonate, Thymol

Questions?

OTC - QUESTIONS SECTION

Gopaldas Visram and Company Limited.

Address - A/327, TTC Industrial Area,

MIDC Mahape, Navi Mumbai,

Maharashtra 400710, India

Zinc Oxide, Menthol and White Petrolatum

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2728580menthol 0.44 % / petrolatum, white 66.625 % / zinc oxide 20.625 % Topical OintmentPSN3
2728580menthol 0.0044 MG/MG / petrolatum 0.666 MG/MG / zinc oxide 0.206 MG/MG Topical OintmentSCD3
2728580menthol 0.0044 MG/MG / petrolatum 0.666 MG/MG / ZNO 0.206 MG/MG Topical OintmentSY3
2728580menthol 0.44 % / petrolatum, white 66.625 % / zinc oxide 20.625 % Topical OintmentSY3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87236-008-04Zinc Oxide with Menthol and White Petrolatum113 g in 1 TUBEOINTMENT1133
87236-008-04Zinc Oxide with Menthol and White Petrolatum1 in 1 BOXOINTMENT13
87236-008-05Zinc Oxide with Menthol and White Petrolatum5 g in 1 PACKETOINTMENT53
87236-008-13Zinc Oxide with Menthol and White Petrolatum113 g in 1 TUBEOINTMENT1133
87236-008-44Zinc Oxide with Menthol and White Petrolatum5 g in 1 PACKETOINTMENT53
87236-008-44Zinc Oxide with Menthol and White Petrolatum144 in 1 CARTONOINTMENT1443

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87236-00887236-008-04, 87236-008-13, 87236-008-05, 87236-008-44

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22026-01-23monthly-update2026-06-03 17:53:08
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 with Menthol and White PetrolatumMENTHOL, ZINC OXIDE, WHITE PETROLATUMAldermed Inc.f993fc0a-bd80-4345-a948-65ac03f910e22026-05-04WarningsExact identifier
ndc (package): 87236-008-04
ndc (package): 87236-008-13
ndc (package): 87236-008-44
ndc (package): 87236-008-05
ndc (product): 87236-008
ndc11 (package): 87236000844
ndc11 (package): 87236000805
ndc11 (package): 87236000813
ndc11 (package): 87236000804
spl id: 5102cba5-d73c-0fea-e063-6294a90a4305
spl set id: f993fc0a-bd80-4345-a948-65ac03f910e2

Reported adverse events (FAERS/openFDA)#

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