189 Vitamin A&D Skin Protectant Ointment

Manufacturer
Medline Industries, LP
Effective date
2024-10-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:25:58

Label at a glance#

ProductMedline
Active ingredientPETROLATUM
Label structure12 sections

Indications and uses

temporarily protects minor cuts, scrapes and burns helps prevent and temporarily protects and helps relieve chapped or cracked skin and lips

Dosage and administration

for skin protectant: apply as needed

Storage and handling

protect from freezing avoid excessive heat

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

White petrolatum 93.4% w/w

Purpose

OTC - PURPOSE SECTION

Skin Protectant

Uses

INDICATIONS & USAGE SECTION

  • temporarily protects minor cuts, scrapes and burns
  • helps prevent and temporarily protects and helps relieve chapped or cracked skin and lips

Warnings

WARNINGS SECTION

For external use only

Do not use on

OTC - DO NOT USE SECTION

  • deep or puncture wounds
  • animal bites
  • serious burns

When using this product

OTC - WHEN USING SECTION

  • do not get into eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens
  • symptoms last for more than 7 days or clear up and occur again within a few days

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

for skin protectant: apply as needed

Other information

STORAGE AND HANDLING SECTION

  • protect from freezing
  • avoid excessive heat

Inactive ingredients

INACTIVE INGREDIENT SECTION

corn oil, mineral oil, vitamin A palmitate (retinyl palmitate), vitamin D

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2601369petrolatum 93.4 % Topical OintmentPSN2
2601369petrolatum 0.934 MG/MG Topical OintmentSCD2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53329-189-44Medline113 g in 1 TUBEOINTMENT1132

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53329-189MEDLINE (WHITE PETROLATUM) OINTMENT [MEDLINE INDUSTRIES, LP]2Current NDC, 1 package rows20241017_e1089e9a-ecaa-5c65-e053-2995a90a8699.zip

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
53329-18953329-189-44

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

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
MedlineWHITE PETROLATUMMedline Industries, LPe1089e9a-ecaa-5c65-e053-2995a90a86992024-10-10WarningsExact identifier
ndc (package): 53329-189-44
ndc (product): 53329-189
ndc11 (package): 53329018944
spl id: 24239268-11f7-361a-e063-6294a90a02d7
spl set id: e1089e9a-ecaa-5c65-e053-2995a90a8699

Reported adverse events (FAERS/openFDA)#

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