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

Warnings
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 than 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 right away.

DOSAGE & ADMINISTRATION SECTION

Directions
Apply as needed.

OTHER SAFETY INFORMATION

Other Information
• Store at controlled room temperature 59º to 86º F (15º to 30º C).

• 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 68599-1186-3

McKesson

Skin Protectant Ointment

With Vitamin A&D

Temporarily protects chapped or cracked skin

Net Wt

4 oz

(113g)

MFR# 118-8719

Not made with natural rubber latex

Satisfaction Guaranteed

Distributed by McKesson Medical-Surgical Inc

Richmond, VA 23233

Rev. 01 06/16 Made in USA

8719 each8719 each

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68599-118668599-1186-3

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
f1637e72-6270-2b1e-e053-2995a90a5b735bd694f8-b5fe-3ee6-e053-2a91aa0acfa32023-01-03WarningsExact identifier
spl id: f1637e72-6270-2b1e-e053-2995a90a5b73
spl set id: 5bd694f8-b5fe-3ee6-e053-2a91aa0acfa3

Reported adverse events (FAERS/openFDA)#

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