MG217 ECZEMA FACE- colloidal oatmeal lotion

MG217 Eczema Face by

Drug Labeling and Warnings

MG217 Eczema Face by is a Otc medication manufactured, distributed, or labeled by Wisconsin Pharmacal Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient

Colloidal Oatmeal (Oat Kernel Flour) 2%

PURPOSE

Purpose

Skin Protectant

INDICATIONS & USAGE

Uses

Temporarily protects and helps relieve minor skin irritation and itching due to

• eczema
• rash
• dermatitis

WARNINGS

For external use only

WHEN USING

When using this product Do not get into eyes

ASK DOCTOR

Stop using and ask doctor if:

condition worsens

symptoms last more than 7 days or clear up and occur again within a few days.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center immediately

DOSAGE & ADMINISTRATION

Directions

Apply as needed, especially after bathing. Massage thoroughly into skin as colloidal oatmeal is slow to absorb.

OTHER SAFETY INFORMATION

Other Information

Keep cap tightly closed when not in use. Store at room temperature. Safe for diabetic skin

INACTIVE INGREDIENT

Inactive ingredients

Purified Water, Cetyl Alcohol, Glycerin, Cetearyl Alcohol, Dicetylphosphate, Ceteth-10 Phosphate, Isopropyl Myristate, Butyrospermum Parkii (Shea Butter), Glucono Delta Lactone, Glyceryl Monolaurate, D-Panthenol, Xanthan Gum, Hydroxypropyl Bispalmitamide MEA, Hydroxyethyl Behenamido-propyl Dimonium Chloride, Palmitic Acid, Conjugated Linoleic Acid, Cholesterol, Euphorbia Cerifera (Candelilla) Wax, Phenoxyethanol, Ethylhexyl Glycerin, Allantoin, Feruloyl Soy Glycerides, Glycyrrhizic Acid, Sodium Benzoate, Sodium Hydroxide, Menthol, Disodium EDTA

QUESTIONS

Questions or comments?

1-800-635-3696

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MG217 ECZEMA FACE 
colloidal oatmeal lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68093-7245
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OATMEAL (UNII: 8PI54V663Y) (OATMEAL - UNII:8PI54V663Y)	OATMEAL	0.02 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
ISOSTEARYL FERULATE (UNII: 877Z5JO557)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
EDETATE DISODIUM (UNII: 7FLD91C86K)
DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N)
CETETH-10 PHOSPHATE (UNII: 4E05O5N49G)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
DEXPANTHENOL (UNII: 1O6C93RI7Z)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
GLUCONOLACTONE (UNII: WQ29KQ9POT)
GLYCERYL 1-LAURATE (UNII: WR963Y5QYW)
XANTHAN GUM (UNII: TTV12P4NEE)
HYDROXYPROPYL BISPALMITAMIDE MONOETHANOLAMIDE (UNII: EVX7NC9YVE)
HYDROXYETHYL BEHENAMIDOPROPYL DIMONIUM CHLORIDE (UNII: 9CO8OUL4TH)
PALMITIC ACID (UNII: 2V16EO95H1)
CHOLESTEROL (UNII: 97C5T2UQ7J)
CETYL ALCOHOL (UNII: 936JST6JCN)
CONJUGATED LINOLEIC ACID (UNII: G199I91G4B)
CANDELILLA WAX (UNII: WL0328HX19)
ALLANTOIN (UNII: 344S277G0Z)
GLYCYRRHIZIN (UNII: 6FO62043WK)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
MENTHOL, (+)- (UNII: C6B1OE8P3W)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
SHEA BUTTER (UNII: K49155WL9Y)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68093-7245-1	170 g in 1 TUBE; Type 0: Not a Combination Product	03/01/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	03/01/2016

Labeler - Wisconsin Pharmacal Company (800873986)

Establishment
Name	Address	ID/FEI	Business Operations
Wisconsin Pharmacal Company		800873986	manufacture(68093-7245)