Label: CAREONE MILK OF MAGNESIA CHERRY- magnesium hydroxide liquid
- NDC Code(s): 72476-665-05
- Packager: Retail Business Services, LLC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not 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 April 22, 2022
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT(S)
- PURPOSE
- USE(S)
- WARNINGS
- ASK A DOCTOR BEFORE USE IF
- ASK A DOCTOR OR PHARMACIST BEFORE USE IF YOU ARE
- STOP USE AND ASK DOCTOR IF
- IF PREGNANT OR BREAST-FEEDING
- KEEP OUT OF REACH OF CHILDREN
-
DIRECTIONS
- shake well before
- do not exceed the maximum recommended daily dose in a 24 hour period
- dose may be taken once a day preferably at bedtime, in divided doses, or as directed by a doctor. Drink a full glass (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 30 mL to 60 mL children 6 to 11 years 15 mL to 30 mL children under 6 years ask a doctor - OTHER INFORMATION
- INACTIVE INGREDIENTS
- PRINCIPLE DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
CAREONE MILK OF MAGNESIA CHERRY
magnesium hydroxide liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72476-665 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Magnesium Hydroxide (UNII: NBZ3QY004S) (MAGNESIUM CATION - UNII:T6V3LHY838) Magnesium Hydroxide 1200 mg in 15 mL Inactive Ingredients Ingredient Name Strength ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) D&C red No. 28 (UNII: 767IP0Y5NH) GLYCERIN (UNII: PDC6A3C0OX) HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) (UNII: S38J6RZN16) water (UNII: 059QF0KO0R) Sodium Hypochlorite (UNII: DY38VHM5OD) Sucrose (UNII: C151H8M554) Product Characteristics Color PINK Score Shape Size Flavor CHERRY Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72476-665-05 355 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/22/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part334 04/22/2022 Labeler - Retail Business Services, LLC. (967989935) Establishment Name Address ID/FEI Business Operations Guardian Drug Company 119210276 MANUFACTURE(72476-665)
