FDA.reportPublic FDA data

First Aid A and D - Walgreen Company

Manufacturer
Walgreen Company
Effective date
2026-07-22
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
daily-update
Hydrated at
2026-07-25 05:10:05

Label at a glance#

ProductFirst Aid A and D
Active ingredientLANOLIN, PETROLATUM
Label structure10 sections

Indications and uses

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

Dosage and administration

for skin protectant use: apply as needed

Label contents#

Full prescribing information#

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Lanolin 15.5%

Petrolatum 53.4%

Purpose

OTC - PURPOSE SECTION

Skin protectant

Skin protectant

Uses

INDICATIONS & USAGE SECTION

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

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 more than 7 days or clear up and occur again within a few days

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OVERDOSAGE SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • for skin protectant use: apply as needed

Other information

OTHER SAFETY INFORMATION

storage temperature: not to exceed 30° C (86° F).

Inactive ingredients

INACTIVE INGREDIENT SECTION

carrot oil, cod liver oil (contains Vitamin A and D), fragrance, light mineral oil, microcrystalline wax, paraffin

Questions?

OTC - QUESTIONS SECTION

1-800-925-4733

SPL UNCLASSIFIED SECTION

DISTRIBUTED BY: WALGREEN CO.

DEERFIELD, IL 60015

Walgreens 100% SATISFACTION GUARANTEED

walgreens.com

©2024 Walgreen Co.

†Our pharmacists recommend the Walgreens brand. We invite you to compare to national brands.

††This product is not manufactured or distributed by Bayer HealthCare LLC, owner of the registered trademark A+D®.

NDC 0363-5362-07

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Walgreens

Walgreens Pharmacist Recommended†

Compare to the active ingredients in A+D® First Aid Ointment††

First Aid A&D Ointment

LANOLIN 15.5%, PETROLATUM 53.4% / SKIN PROTECTANT

  • Temporarily protects minor cuts, scrapes & burns
  • Temporarily protects & helps prevent & relieve chapped, chafed or cracked skin
  • NET WT 4 OZ (113 g)

Walgreen LabelWalgreen Label

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
0363-53620363-5362-07

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
LANOLIN7EV65EAW6HACTIB
PETROLATUM4T6H12BN9UACTIB
MICROCRYSTALLINE WAXXOF597Q3KYIACT
CARROT SEED OIL595AO13F11IACT
PARAFFINI9O0E3H2ZEIACT
LIGHT MINERAL OILN6K5787QVPIACT
COD LIVER OILBBL281NWFGIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22025-10-31full-release2026-06-01 01:17:02

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
First Aid A and DLANOLIN 15.5%, PETROLATUM 53.4%Walgreen Company25a319d0-d39a-5ff0-e063-6394a90a671d2026-07-22WarningsExact identifier
ndc (package): 0363-5362-07
ndc (product): 0363-5362
ndc11 (package): 00363536207
spl id: 5734c13a-dd44-e54a-e063-6294a90a891d
spl set id: 25a319d0-d39a-5ff0-e063-6394a90a671d

Reported adverse events (FAERS/openFDA)#

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