Label: MEDIQUE BAN-ACID MAXIMUM STRENGTH 750- calcium carbonate tablet, chewable
- NDC Code(s): 47682-285-33, 47682-285-36, 47682-285-99
- Packager: Unifirst First Aid Corporation
- 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 July 12, 2022
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- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- Warnings
- DO NOT USE
- ASK DOCTOR
- WHEN USING
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- OTHER SAFETY INFORMATION
- INACTIVE INGREDIENT
- QUESTIONS
-
Medique Ban-acid Label
Medique®
Ban-acid
Maximum Strength 750
Calcium Rich Extra Strength Antacid
Antiacido extra fuerte y /ricas en calcio
Pull To Open
Tire Para Abrir
√ Heartburn, Indigestion,•Calcium Carbonate 750mg
las agruras, la indigestion•Carbonato de Caldo 750mg
Assorted Berry
Bayas surtidas
100
Tablets
(50 x 2)
Tamper Evident Unit Dose Packets
Empaquetado con Sellado Evidente en Dosis Unitarias
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INGREDIENTS AND APPEARANCE
MEDIQUE BAN-ACID MAXIMUM STRENGTH 750
calcium carbonate tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:47682-285 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CARBONATE 750 mg Inactive Ingredients Ingredient Name Strength MINERAL OIL (UNII: T5L8T28FGP) DEXTROSE (UNII: IY9XDZ35W2) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FD&C RED NO. 40 (UNII: WZB9127XOA) MAGNESIUM STEARATE (UNII: 70097M6I30) MALTODEXTRIN (UNII: 7CVR7L4A2D) Product Characteristics Color red (RED) , purple (PURPLE) , gray (GRAY) Score no score Shape ROUND (ROUND) Size 15mm Flavor STRAWBERRY (Blueberry Blackberry) Imprint Code RH;031 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:47682-285-33 50 in 1 BOX 09/29/2017 1 2 in 1 PACKET; Type 0: Not a Combination Product 2 NDC:47682-285-99 2 in 1 PACKET; Type 0: Not a Combination Product 07/01/2014 3 NDC:47682-285-36 75 in 1 BOX 04/01/2019 3 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 07/01/2014 Labeler - Unifirst First Aid Corporation (832947092)