CUREFINI- petrolatum, cod liver ointment

CUREFINI by

Drug Labeling and Warnings

CUREFINI by is a Otc medication manufactured, distributed, or labeled by Rev Pharma Corp., Pure Source, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

CUREFINI Dermal Ointment for cuts & burns SKIN PROTECTION OINTMENT

Active Ingredients

• Petrolatum 30.00%

• Cod Liver Oil 10.00%

Purpose

Skin Protectant

Use For:

• Temporarily protects minor cuts, scrapes and burns.
• Temporarily protects chapped or cracked skin.
• Helps protect from drying effects of wind and cold weather. 

Warnings

• For external use only
• When using this product, do not get into eyes
• If conditions worsens or does not improve for seven days, discontinue use and consult a physician
• Do not use if tamper evident seal is broken

Keep out of reach of children.

• If swallowed, contact physician or poison control center immediately.

STORAGE AND HANDLING

Store at room temperature.

Directions:

• Apply as needed. Prepare a gauze bandage to apply. Dressing should be placed on a clean and flat surface. Apply ointment with spatula, covering the entire surface with a thin layer. Place bandage directly on top of affected area. Make sure affected area remains covered by ointment. 

Other Ingredients:

beeswax, BHT, Sunflower oil, Sweet almond oil

CUREFINI 8oz/240ml (65121-712-65)

INGREDIENTS AND APPEARANCE

CUREFINI 
petrolatum, cod liver ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69981-712
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U)	PETROLATUM	300 mg  in 1 mL
COD LIVER OIL (UNII: BBL281NWFG) (COD LIVER OIL - UNII:BBL281NWFG)	COD LIVER OIL	100 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
YELLOW WAX (UNII: 2ZA36H0S2V)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
SUNFLOWER OIL (UNII: 3W1JG795YI)
ALMOND OIL (UNII: 66YXD4DKO9)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69981-712-65	240 mL in 1 JAR; Type 0: Not a Combination Product	01/17/2013
2	NDC: 69981-712-64	120 mL in 1 JAR; Type 0: Not a Combination Product	01/17/2013

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	01/17/2013

Labeler - Rev Pharma Corp. (079422405)

Establishment
Name	Address	ID/FEI	Business Operations
Pure Source, LLC		080354456	manufacture(69981-712)