Label: PHILLIPS MILK OF MAGNESIA CONCENTRATED FRESH STRAWBERRY liquid
- NDC Code(s): 0280-0033-09
- Packager: Bayer HealthCare LLC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 30, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- PURPOSE
- Use
- WARNINGS
- DO NOT USE
- Ask a doctor before use if you have
- ASK DOCTOR/PHARMACIST
- Stop use and ask a doctor if
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
-
Directions
- do not exceed the maximum recommended daily dose in a 24 hour period
- shake well before use
- dose may be taken once a day preferably at bedtime, in divided doses, or as directed by a doctor. Drink a full glas (8 oz) of liquid with each dose.
- for accurate dosing, only use the dosing cup provided
- mL = milliliter
- Adults and children 12 years and older: 15 mL to 30 mL
- Children under 12 years: ask a doctor
- Other information
- Inactive ingredients
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
PHILLIPS MILK OF MAGNESIA CONCENTRATED FRESH STRAWBERRY
phillips milk of magnesia concentrated fresh strawberry liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0280-0033 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM HYDROXIDE 2400 mg in 15 mL Inactive Ingredients Ingredient Name Strength SODIUM HYPOCHLORITE (UNII: DY38VHM5OD) SORBITOL SOLUTION (UNII: 8KW3E207O2) WATER (UNII: 059QF0KO0R) SUCROSE (UNII: C151H8M554) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) D&C RED NO. 28 (UNII: 767IP0Y5NH) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) Product Characteristics Color Score Shape Size Flavor STRAWBERRY Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0280-0033-09 237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/20/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M007 12/18/2014 Labeler - Bayer HealthCare LLC. (112117283)