FDA.reportPublic FDA data

Cherry Antacid Soft Chew

Manufacturer
Family Dollar | Bestco Inc.
Effective date
2018-01-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:04:14

Label at a glance#

ProductCherry Antacid Soft Chew
Active ingredientCALCIUM CARBONATE
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient (in each chew)

Calcium Carbonate 1177 mg

OTC - PURPOSE SECTION

Purpose

Antacid

INDICATIONS & USAGE SECTION

Uses: Relieves

heartburn

sour stomach

acid indigestion

upset stomach die to these symptoms

WARNINGS SECTION

Warnings

Ask a doctor or pharmacist before use if you are now taking a prescription drug. Antacids may interact with certain prescription drugs.

OTC - WHEN USING SECTION

When using this product do not take more than 6 chews in a 24-hour period, or use the maximum dosage for more than 2 weeks, except under the advice and supervision of a physician.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If you are pregnant or breast-feeding, ask a doctor before using this product.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

Directions

Chew and swallow 2 to 3 chews, as symptoms occur or as directed by a physician.

OTHER SAFETY INFORMATION

Other information

Each chew contains: calcium 470 mg, magnesium 5 mg

Contains milk and soy

INACTIVE INGREDIENT SECTION

Inactive ingredients: Corn starch, corn syrup, corn syrup solids, FD&C red no. 40 aluminum lake, glycerin, hydrogenated coconut oil, medium chain triglycerides, natural and artificial flavors, non-fat dried milk power, soybean oil, soy lecithin and sucrose.

OTC - QUESTIONS SECTION

Questions? Or to report an adverse event call 1-800-245-2898. Monday - Friday, 9AM to 4PM EST

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Family Wellness Cherry Antacid SC 32ctFamily Wellness Cherry Antacid SC 32ct

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
55319-016-322022-06-30C16284748780-19d75b9d0-ed2e-f424-e053-dadaa90a57ceCalcium Carbonate 1177 mg
55319-016-322020-01-31C16284748780-19d75b9d0-ed2e-f424-e053-dadaa90a57ceCalcium Carbonate 1177 mg

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55319-01655319-016-32

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
CALCIUM CARBONATEH0G9379FGKACTIB
SUCROSEC151H8M554IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
e2affcdf-7257-8f44-e053-2995a90a2d1863a11550-3885-ac02-e053-2991aa0af56d2022-06-30WarningsExact identifier
spl set id: 63a11550-3885-ac02-e053-2991aa0af56d

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.