FDA.reportPublic FDA data

Maximum Strength Moisture Barrier Ointment

Manufacturer
Derma Sciences Canada Inc.
Effective date
2025-10-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:41:16

Label at a glance#

ProductMaximum Strength Moisture Barrier
Active ingredientPETROLATUM, ZINC OXIDE
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Petrolatum 50%

Zinc Oxide 16%

OTC - ASK DOCTOR SECTION

Discontinue use and contact a physician if condition worsens.

INDICATIONS & USAGE SECTION

Uses

Temporarily protects and helps relieve minor skin irritation and itching due to rashes

DOSAGE & ADMINISTRATION SECTION

Directions

  • Carefully cleanse the area and pat dry thoroughly. Apply liberally to desired areas as often as necessary.

WARNINGS SECTION

Warnings

Keep out of reach of children. For external use only. Avoid Eye contact. Discontinue use and contact a physician if condition worsens.

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Flower Extract, DMDM Hydantoin; Hydrogenated Castor Oil; Myroxylon Balsamum, Vitamin A Palminate, Vitamin D, Vitamin E (Alpha Tocopherol)

OTC - PURPOSE SECTION

Skin Protectant

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

OTC - QUESTIONS SECTION

1-800-840-9041

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Maximum Moisture Barrier OintmentMaximum Moisture Barrier Ointment

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2727316petrolatum 50 % / zinc oxide 16 % Topical OintmentPSN1
2727316petrolatum 0.5 MG/MG / zinc oxide 0.16 MG/MG Topical OintmentSCD1
2727316petrolatum 0.5 MG/MG / ZNO 0.16 MG/MG Topical OintmentSY1
2727316petrolatum 50 % / zinc oxide 16 % Topical OintmentSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64772-203-01Maximum Strength Moisture Barrier113.4 g in 1 TUBEOINTMENT113.41

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64772-20364772-203-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE BARBADENSIS LEAF JUICERUE8E6T4NBIACT
PETROLATUM4T6H12BN9UACTIB
VITAMIN D9VU1KI44GPIACT
MYROXYLON BALSAMUM WHOLE5OU0811D9JIACT
.ALPHA.-TOCOPHEROL ACETATE, D-A7E6112E4NIACT
DMDM HYDANTOINBYR0546TOWIACT
VITAMIN A PALMITATE1D1K0N0VVCIACT
ZINC OXIDESOI2LOH54ZACTIB
HYDROGENATED CASTOR OILZF94AP8MEYIACT

Source Document#

Source XML

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
Maximum Strength Moisture BarrierPETROLATUM AND ZINC OXIDEDerma Sciences Canada Inc.41ee91c0-d196-cc0f-e063-6394a90a7b972025-10-24WarningsExact identifier
ndc (package): 64772-203-01
ndc (product): 64772-203
ndc11 (package): 64772020301
spl id: 41ee91c0-d197-cc0f-e063-6394a90a7b97
spl set id: 41ee91c0-d196-cc0f-e063-6394a90a7b97

Reported adverse events (FAERS/openFDA)#

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