HARMON FACE VALUES ADVANCED SEVERE DRY SKIN THERAPY- petrolatum ointment

Harmon Face Values Advanced by

Drug Labeling and Warnings

Harmon Face Values Advanced by is a Otc medication manufactured, distributed, or labeled by Delta Pharma Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient

Petrolatum (41%)

PURPOSE

Purpose

Skin Protectant (ointment)

INDICATIONS & USAGE

Uses

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

WARNINGS

Warning
For external use only

WHEN USING

When using this product, do not get into eyes

STOP USE

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
  

DO NOT USE

Do not use on

• deep or puncture wounds
• animal bites
• serious burns
  

KEEP OUT OF REACH OF CHILDREN

Keep out of the reach of children.

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

DOSAGE & ADMINISTRATION

Directions

Apply as needed

INACTIVE INGREDIENT

Inactive Ingredients

Mineral Oil, Ceresin, Lanolin Alcohol, Panthenol, Glycerin, Bisabolol

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HARMON FACE VALUES ADVANCED   SEVERE DRY SKIN THERAPY
petrolatum ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66353-100
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Petrolatum (UNII: 4T6H12BN9U) (Petrolatum - UNII:4T6H12BN9U)	Petrolatum	41 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
Mineral Oil (UNII: T5L8T28FGP)
Ceresin (UNII: Q1LS2UJO3A)
LANOLIN ALCOHOLS (UNII: 884C3FA9HE)
Panthenol (UNII: WV9CM0O67Z)
Glycerin (UNII: PDC6A3C0OX)
LEVOMENOL (UNII: 24WE03BX2T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66353-100-10	2 in 1 CARTON	11/21/2011
1		10 g in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 66353-100-01	50 g in 1 TUBE; Type 0: Not a Combination Product	11/21/2011

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	11/21/2011

Labeler - Delta Pharma Inc. (200161730)

Establishment
Name	Address	ID/FEI	Business Operations
Delta Pharma Inc.		200161730	manufacture(66353-100)