FDA.reportPublic FDA data

McKesson Skin Protectant Ointment

Manufacturer
McKesson | Ultra Seal Corporation
Effective date
2023-01-03
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
legacy-cache
Hydrated at
2026-08-01 21:41:54

Label at a glance#

ProductSkin Protectant
Active ingredientPETROLATUM
Label structure13 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient (in each gram)

White Petrolatum 93.5%

OTC - PURPOSE SECTION

Purpose

Skin Protectant

INDICATIONS & USAGE SECTION

Uses

temporarily relieves minor cuts, scrapes, burns
temporarily protects and helps relieve chapped or cracked skin and lips
helps protect from the effects of wind and cold weather

WARNINGS SECTION

Warning

For external use only.

When using this product

  • do not get into eyes

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • condition worsens
  • a rash or allergic reaction develops
  • symptoms last more that 7 days or clear up and occur again within a few days

OTC - DO NOT USE SECTION

Do not use on

  • deep or puncture wounds
  • animal bites
  • serious burns

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center righ away

DOSAGE & ADMINISTRATION SECTION

Directions

Apply as needed.

OTHER SAFETY INFORMATION

Other information

  • Store at controlled room temperature 59-86ºF (15-30ºC).
  • Avoid excessive heat and humidity.

INACTIVE INGREDIENT SECTION

Inactive ingredients

Corn Oil, Light Mineral Oil, Vitamin A Palmitate, Vitamin D

OTC - QUESTIONS SECTION

Questions? Call 1-800-777-4908

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 68599-1185-7

McKesson

Skin Protectant Ointment

With Vitamins A&D

Temporarily protects chapped or cracked skin

Net Wt.

13 oz

(368.5g)

MFR#188-8712

Not made with natural rubber latex

Satisfaction Guaranteed

Distributed by McKesson Medical-Surgical Inc.

Richmond, VA 23233 Rev. 02 06/16 Made in USA

8712 each8712 each

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68599-118568599-1185-7

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
CORN OIL8470G57WFMIACT
LIGHT MINERAL OILN6K5787QVPIACT
VITAMIN D9VU1KI44GPIACT
VITAMIN A PALMITATE1D1K0N0VVCIACT
PETROLATUM4T6H12BN9UACTIB

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
f1635e9d-d19a-883f-e053-2a95a90a54a85bd276f2-52c2-1754-e053-2991aa0a35772023-01-03WarningsExact identifier
spl id: f1635e9d-d19a-883f-e053-2a95a90a54a8
spl set id: 5bd276f2-52c2-1754-e053-2991aa0a3577

Reported adverse events (FAERS/openFDA)#

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