MG217 BABY ECZEMA- colloidal oatmeal lotion

MG217 Baby Eczema by

Drug Labeling and Warnings

MG217 Baby Eczema 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 wtihin 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.

INACTIVE INGREDIENT

Inactive ingredients

Purified Water, Cetyl Alcohol, Glycerin, Cetearyl Alcohol, Dicetylphosphate, Ceteth-10 Phosphate, Isopropyl Myristate, Persea Gratissima (Avocado) Oil, Glucono Delta Lactone, Glyceryl Monolaurate, D-Panthenol, Xanthan Gum, Hydroxypropyl Bispalmitamide MEA, Hydroxyethyl Behenamidopropyl Dimonium Chloride, Palmitic Acid, Conjugated Linoleic Acid, Cholesterol, Euphorbia Cerifera (Candelilla) Wax, Phenoxyethanol, Ethylhexyl Glycerin, Allantoin, Glycyrrhizic Acid, Sodium Benzoate, Sodium Hydroxide, Menthol, Disodium EDTA

QUESTIONS

Questions or comments?

1-800-635-3696

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MG217 BABY ECZEMA 
colloidal oatmeal lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68093-5105
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
CETYL ALCOHOL (UNII: 936JST6JCN)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
ALLANTOIN (UNII: 344S277G0Z)
GLYCYRRHIZIN (UNII: 6FO62043WK)
GLYCERYL 1-LAURATE (UNII: WR963Y5QYW)
HYDROXYETHYL BEHENAMIDOPROPYL DIMONIUM CHLORIDE (UNII: 9CO8OUL4TH)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
HYDROXYPROPYL BISPALMITAMIDE MONOETHANOLAMIDE (UNII: EVX7NC9YVE)
DEXPANTHENOL (UNII: 1O6C93RI7Z)
GLUCONOLACTONE (UNII: WQ29KQ9POT)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N)
CANDELILLA WAX (UNII: WL0328HX19)
CETETH-10 PHOSPHATE (UNII: 4E05O5N49G)
EDETATE DISODIUM (UNII: 7FLD91C86K)
WATER (UNII: 059QF0KO0R)
MENTHOL, (+)- (UNII: C6B1OE8P3W)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
AVOCADO OIL (UNII: 6VNO72PFC1)
SODIUM BENZOATE (UNII: OJ245FE5EU)
GLYCERIN (UNII: PDC6A3C0OX)
XANTHAN GUM (UNII: TTV12P4NEE)
PALMITIC ACID (UNII: 2V16EO95H1)
CONJUGATED LINOLEIC ACID (UNII: G199I91G4B)
CHOLESTEROL (UNII: 97C5T2UQ7J)
PHENOXYETHANOL (UNII: HIE492ZZ3T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68093-5105-1	170 g in 1 TUBE; Type 0: Not a Combination Product	02/01/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	02/01/2016

Labeler - Wisconsin Pharmacal Company (800873986)

Establishment
Name	Address	ID/FEI	Business Operations
Wisconsin Pharmacal Company		800873986	manufacture(68093-5105)