LANOLIN 50%- lanolin cream

Drug Labeling and Warnings

Drug Details [pdf]

Active Ingredient

Lanolin USP 50%

Purpose

Skin Protectant

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

Warnings

For external use only

Do not use on

• deep or puncture wounds
• animal bites
• serious burns

When using this product

• do not get into eyes

Stop use and ask a doctor if

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

If pregnant or breast-feeding

ask a health professional before use.

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

Directions

apply as needed

Other 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

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

Questions

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

Label

INGREDIENTS AND APPEARANCE

LANOLIN 50% 
lanolin cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87236-019
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LANOLIN (UNII: 7EV65EAW6H) (LANOLIN - UNII:7EV65EAW6H)	LANOLIN	50 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
POLYSORBATE 60 (UNII: CAL22UVI4M)
PETROLATUM (UNII: 4T6H12BN9U)
SODIUM BORATE (UNII: 91MBZ8H3QO)
LANOLIN ALCOHOLS (UNII: 884C3FA9HE)
EDETATE DISODIUM (UNII: 7FLD91C86K)
WATER (UNII: 059QF0KO0R)
WHITE WAX (UNII: 7G1J5DA97F)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87236-019-04	113 g in 1 TUBE; Type 0: Not a Combination Product	12/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	12/01/2025

Labeler - Aldermed Inc. (144887712)