Black & White Skin Protectant Ointment

Manufacturer
J. Strickland & Co.
Effective date
2025-11-07
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
monthly-update
Hydrated at
2026-06-03 17:39:35

Label at a glance#

ProductBlack and White Skin Protectant
Active ingredientPETROLATUM
Label structure6 sections

Indications and uses

Temporarily protects minor cuts scrapes burns chapped or cracked skin

Dosage and administration

Apply as needed.

Label contents#

Full prescribing information#

Active Ingredients:

OTC - ACTIVE INGREDIENT SECTION

Petrolatum, 62%

Purpose

OTC - PURPOSE SECTION

Skin Protectant

Uses:

INDICATIONS & USAGE SECTION

Temporarily protects minor

  • cuts
  • scrapes
  • burns
  • chapped or cracked skin

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 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

  • If swallowed, get medical help or call a poison control center at once.

Directions:

DOSAGE & ADMINISTRATION SECTION

  • Apply as needed.

Other Ingredients:

INACTIVE INGREDIENT SECTION

Beta Carotene, D&C Green 6, D&C Red 17, Glycerin, Hydrogenated Vegetable Oil, Lanolin, Microcrystalline Wax, Ozokerite, Resorcinol, Synthetic Bees-wax, Turpentine.

Package Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

12022-004-0012022-004-00

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130075610947106GTIN-13: 0075610947106
EAN-13: 0075610947106
GTIN-12: 075610947106
UPC-A: 075610947106
GTIN storage (14 digits): 00075610947106
12022-004-00.jpg

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
12022-00412022-004-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22023-10-21full-release2026-05-31 23:58:36

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
43042904-ac42-6398-e063-6394a90ac283fcf83c55-cc9b-4017-8fb7-365cc4aa09712025-11-07WarningsExact identifier
spl id: 43042904-ac42-6398-e063-6394a90ac283
spl set id: fcf83c55-cc9b-4017-8fb7-365cc4aa0971

Reported adverse events (FAERS/openFDA)#

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