Label: NUTRALOX- calcium carbonate tablet, chewable
-
Contains inactivated NDC Code(s)
NDC Code(s): 50332-0106-1, 50332-0106-3, 50332-0106-4, 50332-0106-7, view more50332-0106-8 - Packager: HART Health
- Category: HUMAN OTC DRUG LABEL
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 June 5, 2020
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- ASK DOCTOR/PHARMACIST
- STOP USE
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
-
DOSAGE & ADMINISTRATION
Directions:
Do not take more than directed
Adults and children 12 years of age and over:
- thoroughly chew 2 tablets every 3 to 4 hours as symptoms occur
- do not take more than 16 tablets in 24 hours unless directed by a doctor
- do not use the maximum dose for more than 2 weeks
Children under 12 years of age: ask a doctor
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
NUTRALOX
calcium carbonate tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50332-0106 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CARBONATE 420 mg Inactive Ingredients Ingredient Name Strength MAGNESIUM STEARATE (UNII: 70097M6I30) SUCROSE (UNII: C151H8M554) ACACIA (UNII: 5C5403N26O) MALTODEXTRIN (UNII: 7CVR7L4A2D) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) STARCH, CORN (UNII: O8232NY3SJ) Product Characteristics Color white Score no score Shape ROUND Size 12mm Flavor Imprint Code NLX Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50332-0106-3 20 in 1 BOX, UNIT-DOSE 01/20/1987 1 2 in 1 PACKET; Type 0: Not a Combination Product 2 NDC:50332-0106-4 50 in 1 BOX, UNIT-DOSE 01/20/1987 2 2 in 1 PACKET; Type 0: Not a Combination Product 3 NDC:50332-0106-7 125 in 1 BOX, UNIT-DOSE 01/20/1987 3 2 in 1 PACKET; Type 0: Not a Combination Product 4 NDC:50332-0106-8 250 in 1 BOX, UNIT-DOSE 01/20/1987 4 2 in 1 PACKET; Type 0: Not a Combination Product 5 NDC:50332-0106-1 500 in 1 BOX, UNIT-DOSE 01/20/1987 5 2 in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part331 01/20/1987 Labeler - HART Health (069560969)