NDC | 69842-628-12 |
Set ID | 53fc327e-e345-26f2-e054-00144ff8d46c |
Category | HUMAN OTC DRUG LABEL |
Packager | CVS PHARMACY,INC. |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART331 |
- Active ingredients (in each 5 mL teaspoonful)
- Purpose
- Uses
-
Warnings
Ask a doctor before use if you have
- kidney disease
- a magnesium-restricted diet
- a sodium-restricted diet
Ask a doctor or pharmacist before use if you are taking a prescription drug. Antacids may interact with certain prescription drugs.
When using this product
- laxative effect may occur
- do not use maximum dosage for more than 2 weeks
- do not take more than 16 teaspoonfuls in 24 hours
If pregnant or breast-feeding, ask a health professional before use.
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
- package Label
-
INGREDIENTS AND APPEARANCE
EXTRA STRENGTH HEARTBURN RELIEF
aluminum hydroxide and magnesium carbonate suspensionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69842-628 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) (ALUMINUM HYDROXIDE - UNII:5QB0T2IUN0) ALUMINUM HYDROXIDE 254 mg in 5 mL MAGNESIUM CARBONATE (UNII: 0E53J927NA) (CARBONATE ION - UNII:7UJQ5OPE7D) MAGNESIUM CARBONATE 237.5 mg in 5 mL Inactive Ingredients Ingredient Name Strength BENZYL ALCOHOL (UNII: LKG8494WBH) EDETATE DISODIUM (UNII: 7FLD91C86K) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) SACCHARIN SODIUM (UNII: SB8ZUX40TY) SODIUM ALGINATE (UNII: C269C4G2ZQ) SORBITOL (UNII: 506T60A25R) XANTHAN GUM (UNII: TTV12P4NEE) DIMETHICONE (UNII: 92RU3N3Y1O) Product Characteristics Color white Score Shape Size Flavor CHERRY Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69842-628-12 355 mL in 1 BOTTLE; Type 0: Not a Combination Product 02/01/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part331 02/01/2017 Labeler - CVS PHARMACY,INC. (062312574) Registrant - GCP Laboratories (965480861) Establishment Name Address ID/FEI Business Operations GCP Laboratories 965480861 manufacture(69842-628)