FDA.reportPublic FDA data

Walgreens Healing Ointment Petrolatum Skin Protectant

Manufacturer
WALGREEN COMPANY
Effective date
2023-04-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:32:44

Label at a glance#

ProductWalgreens Healing Petrolatum Skin Protectant
Active ingredientPETROLATUM
Label structure12 sections

Indications and uses

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

Dosage and administration

Apply as needed.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Petrolatum 46.5%

Purpose

OTC - PURPOSE SECTION

Skin protectant

Uses

INDICATIONS & USAGE SECTION

  • temporarily protects and helps relieve chapped or cracked skin and lips
  • temporarily protects minor:

• cuts

• scrapes

• burns

  • helps protect from the drying effects of wind and cold weather

Warnings

WARNINGS SECTION

For external use only

When using this product 

OTC - WHEN USING SECTION

• do not get into eyes

Stop use and ask a doctor if

OTC - ASK DOCTOR SECTION

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

Do not use on

OTC - DO NOT USE SECTION

• deep or puncture wounds • animal bites • serious burns

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Apply as needed.

Other information

OTHER SAFETY INFORMATION

  • may stain some fabrics

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Mineral Oil, Paraffin, Ozokerite, Dimethicone, Hyaluronic Acid, Sodium Hydroxide, Ceramide 1, Ceramide 3, Ceramide 6-II, Tocopheryl Acetate, Phytosphingosine, Cholesterol, Sodium Lauroyl Lactylate, Carbomer, Panthenol, Water, L-Proline, Xanthan Gum.

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

W41283A1W41283A1

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-01820363-0182-09

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
PROLINE9DLQ4CIU6VIACT
SODIUM HYDROXIDE55X04QC32IIACT
SODIUM LAUROYL LACTYLATE7243K85WFOIACT
WATER059QF0KO0RIACT
HEXAMETHYLDISILOXANED7M4659BPUIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
CERAMIDE NP4370DF050BIACT
CHOLESTEROL97C5T2UQ7JIACT
HYALURONATE SODIUMYSE9PPT4THIACT
MINERAL OILT5L8T28FGPIACT
PANTHENOLWV9CM0O67ZIACT
PETROLATUM4T6H12BN9UACTIB
POLYACRYLIC ACID (8000 MW)73861X4K5FIACT
CERAMIDE APF1X8L2B00JIACT
CERESINQ1LS2UJO3AIACT
PARAFFINI9O0E3H2ZEIACT
PHYTOSPHINGOSINEGIN46U9Q2QIACT
XANTHAN GUMTTV12P4NEEIACT

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
243b2eaa-41c8-2273-e063-6394a90a7537f9c84959-452c-227f-e053-6394a90a9ad52024-10-11WarningsExact identifier
spl set id: f9c84959-452c-227f-e053-6394a90a9ad5

Reported adverse events (FAERS/openFDA)#

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