LINCOLN- white petrolatum ointment

Lincoln by

Drug Labeling and Warnings

Lincoln by is a Otc medication manufactured, distributed, or labeled by Lincoln Pharmaceuticals Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

White Petrolatum USP (76% w/w)

PURPOSE

Skin Protectant

USES

• helps treat and prevent diaper rash
• helps seal out wetness
• temporarily protects minor cuts, scrapes, burns
• temporarily helps protect and relieve chapped and cracked skin or lips
• helps prevent and protect from the drying effects of wind and cold weather
• helps prevent and protect chafed skin in minor irritations associated with diaper rash
• with each diaper change, especially at bedtime when exposure to wet diapers may be prolonged

WARNINGS:

FOR EXTERNAL USE ONLY

When using this product:

• do not get into eyes

Stop Use and ask a doctor if

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

Do not use on

• deep or puncture wounds
• animal bites
• serious burns

Keep out of reach of children

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

DIRECTIONS

For Diaper Rash:

change wet and soiled diaper promptly
cleanse the diaper area allow to dry
apply as needed

OTHER INFORMATION

• store at room temperature 15° - 30 °C (59-86 F)
• avoid excessive heat and humidity

INACTIVE INGREDIENTS

lanolin, lavender oil, light liquid paraffin, vitamin A, Vitamin D

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LINCOLN 
white petrolatum ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69636-3045
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U)	PETROLATUM	76 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
LAVENDER OIL (UNII: ZBP1YXW0H8)
VITAMIN A (UNII: 81G40H8B0T)
VITAMIN D (UNII: 9VU1KI44GP)
LANOLIN (UNII: 7EV65EAW6H)
LIGHT MINERAL OIL (UNII: N6K5787QVP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69636-3045-2	5 g in 1 PACKET; Type 0: Not a Combination Product	01/10/2017
2	NDC: 69636-3045-3	28.3 g in 1 TUBE; Type 0: Not a Combination Product	01/10/2017
3	NDC: 69636-3045-4	113 g in 1 TUBE; Type 0: Not a Combination Product	01/10/2017
4	NDC: 69636-3045-5	425 g in 1 JAR; Type 0: Not a Combination Product	01/10/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	01/10/2017

Labeler - Lincoln Pharmaceuticals Ltd. (915839373)

Establishment
Name	Address	ID/FEI	Business Operations
Lincoln Pharmaceuticals Ltd.		915839373	manufacture(69636-3045)