Lanolin 50%

Manufacturer: Aldermed Inc.
Effective date: 2026-09-25
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: daily-update
Hydrated at: 2026-09-29 01:03:31

Label at a glance#

ProductLanolin 50%

Active ingredientLANOLIN

Label structure9 sections

Indications and uses

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

Dosage and administration

apply as needed

Contacts and useful links#

PhonePoison Help1-800-222-1222

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Lanolin USP 50%

Purpose

OTC - PURPOSE SECTION

Skin Protectant

Uses

INDICATIONS & USAGE SECTION

• temporarily protects minor: cuts, scrapes, burns
• temporarily protects and helps relieve chafed, chapped or cracked skin and lips
• helps prevent and 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

If pregnant or breast-feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

Directions

DOSAGE & ADMINISTRATION SECTION

apply as needed

Other Information

OTHER SAFETY INFORMATION

to open: unscrew cap, pull tab to remove foil seal
store at 15° to 30°C (59° to 86°F)
avoid excessive heat
see tube crimp for lot number and expiration date

Inactive Ingredients

INACTIVE INGREDIENT SECTION

cetostearyl alcohol, edetate disodium, fragrance, lanolin alcohols, polysorbate 60, purified water, sodium borate, white petrolatum, white wax

Questions

OTC - QUESTIONS SECTION

Call 1-833-605-84-74 9am-5 pm EST M-F

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

tubepackageboxbox

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	0850083488710	GTIN-13: 0850083488710 EAN-13: 0850083488710 GTIN-12: 850083488710 UPC-A: 850083488710 GTIN storage (14 digits): 00850083488710	AMGV0281_Lanolin_50_Cream_4oz_Tube-1.jpg
Barcode	EAN-13	0850083488741	GTIN-13: 0850083488741 EAN-13: 0850083488741 GTIN-12: 850083488741 UPC-A: 850083488741 GTIN storage (14 digits): 00850083488741	AMGV0284_Lanolin_50_Cream_14oz_Jar_Label-1.jpg
Barcode	EAN-13	0850083488758	GTIN-13: 0850083488758 EAN-13: 0850083488758 GTIN-12: 850083488758 UPC-A: 850083488758 GTIN storage (14 digits): 00850083488758	AMGV0285_Lanolin_50_Cream_5g-1.jpg

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

Lanolin 50%
Lanolin
POLYSORBATE 60
PETROLATUM
SODIUM BORATE
LANOLIN ALCOHOLS
EDETATE DISODIUM
WATER
WHITE WAX
CETOSTEARYL ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
87236-019	87236-019-04, 87236-019-05, 87236-019-44, 87236-019-14

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
LANOLIN	7EV65EAW6H	ACTIB
POLYSORBATE 60	CAL22UVI4M	IACT
PETROLATUM	4T6H12BN9U	IACT
SODIUM BORATE	91MBZ8H3QO	IACT
LANOLIN ALCOHOLS	884C3FA9HE	IACT
EDETATE DISODIUM	7FLD91C86K	IACT
WATER	059QF0KO0R	IACT
WHITE WAX	7G1J5DA97F	IACT
CETOSTEARYL ALCOHOL	2DMT128M1S	IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
1	2026-05-07	full-release	2026-06-01 01:56:31

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
513a5bbf-c2d9-9a9a-e063-6394a90af64a			513a5bb2-7879-f007-e063-6394a90a94ff	2026-05-07	Warnings	Exact identifier spl set id: 513a5bb2-7879-f007-e063-6394a90a94ff

Reported adverse events (FAERS/openFDA)#

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