Label: MG217 ECZEMA FACE- colloidal oatmeal lotion
- NDC Code(s): 68093-7245-1
- Packager: Wisconsin Pharmacal Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated November 30, 2017
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- WHEN USING
- ASK DOCTOR
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
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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
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INGREDIENTS AND APPEARANCE
MG217 ECZEMA FACE
colloidal oatmeal lotionProduct 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)