Assorted Fruit Panned Chew

Manufacturer
The Kroger Company | BestCo Inc.
Effective date
2024-11-30
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
legacy-cache
Hydrated at
2026-08-01 20:48:14

Label at a glance#

ProductAssorted Fruit Panned Chew
Active ingredientCALCIUM CARBONATE
Label structure13 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient (in each chewable tablet)

Calcium carbonate 750 mg

OTC - PURPOSE SECTION

Purpose

Antacid

INDICATIONS & USAGE SECTION

Uses: Relieves

  • Heatrburn
  • Sour Stomach
  • Acid indigestion
  • Upset stomach due to these symptoms

WARNINGS SECTION

Warning

Do not use if you have ever had an allergic reaction to this product or any of its ingredients.

Ask a doctor or pharmacist before use if you are now

taking a prescription drug. Antacids may intract with

certain perscription drugs.

Do not take more than 5 chews in a 24-hour period,

or use the maximum dosage formore than 2 weeks,

except under the advice and supervision fo a physician.

OTC - WHEN USING SECTION

When using this product constipation may occur

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional

before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

Directions

Adults and children 12 years and older chew and swallow

1 to 2 chewable tablets every 2-4 hours as needed. Do not exceed 5 chewable tablets

in 24 hours. Children under 12 years consult a doctor.

OTHER SAFETY INFORMATION

Other information

  • Each chewable tablet contains: calcium 300mg
  • Contains: Soy
  • Contains FD&C yellow No.5 (tartrazine) as a color additive
  • Store between 20º to 25º C (68º to 77ºF) in a dry place

INACTIVE INGREDIENT SECTION

Inactive ingredients:

Beeswax, carmine, carnauba wax, citric acid, corn starch, corn syrup,

DL-alpha tocopherol, ethyl acetate, FD&C blue no. 1

aluminum lake, FD&C red no. 40 aluminum lake, FD&C

yellow no. 5 lake (tartrazine), FD&C yellow no. 6, FD&C

yellow no. 6 aluminum lake, gum arabic, hydrogenated

coconut oil, maltodextrin, medium chain triglycerides, methyl paraben,

modified corn starch, natural and artificial flavors, phosphoric acid, pregelatinized corn starch,

propyl paraben, propylene glycol, purified water, shellac, sodium benzoate,

sorbic acid, sorbitol, soy lecithin, soybean oil, sucrose, titanium dioxide.

OTC - QUESTIONS SECTION

Questions? 1-800-632-6900

RECENT MAJOR CHANGES SECTION

Dosage and Administration

Directions

Adults and children 12 years and older chew and swallow

1 to 2 chewable tablets every 2-4 hours as needed. Do not exceed 5 chewable tablets

in 24 hours. Children under 12 years consult a doctor.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Kroger Antacid Fruit Chews 36ctKroger Antacid Fruit Chews 36ct

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
30142-036ASSORTED FRUIT PANNED CHEW (CALCIUM CARBONATE) TABLET, CHEWABLE [THE KROGER COMPANY]7Legacy NDC20241202_437854c0-8c9a-6ef0-e054-00144ff8d46c.zip

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
30142-03630142-036-36

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
CARNAUBA WAXR12CBM0EIZIACT
CALCIUM CARBONATEH0G9379FGKACTIB

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
463b6f6d-874b-dac3-e063-6294a90aeaf2437854c0-8c9a-6ef0-e054-00144ff8d46c2025-12-18WarningsExact identifier
spl set id: 437854c0-8c9a-6ef0-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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