GoodSense Antacid Fruit Chews

Manufacturer
Geiss, Destin, Dunn | Bestco LLC
Effective date
2024-11-30
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 20:48:20

Label at a glance#

ProductGoodSense Antacid Fruit Chews
Active ingredientCALCIUM CARBONATE
Label structure14 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

  • Heartburn
  • Sour stomach
  • Acid indigestion
  • Upset stomach due to these symptoms

WARNINGS SECTION

Warnings

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

OTC - ASK DOCTOR/PHARMACIST SECTION

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

OTC - DO NOT USE SECTION

Do not use the maximum dosage for more than 2 weeks, except under the advice and supervision of a physician.

OTC - WHEN USING SECTION

When using this product constipation may occur.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant of 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 20° to 25° C (68° to 77°F) 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 and titanium dioxide.

OTC - QUESTIONS SECTION

Questions? Call 1-800-245-2898

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

GoodSense Fruit Antacid Chews 32ctGoodSense Fruit Antacid Chews 32ct

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50804-012GOODSENSE ANTACID FRUIT CHEWS (CALCIUM CARBONATE) TABLET, CHEWABLE [GEISS, DESTIN, DUNN]4Legacy NDC20241202_c69f07b1-660a-db03-e053-2995a90a5464.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50804-012-32EA - Each50804-012f3893ce8-0d16-453a-817a-23b8c7c530c112024-03-12

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
50804-01250804-012-32

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
WATER059QF0KO0RIACT

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
3f163419-1771-4113-e063-6294a90a102cc69f07b1-660a-db03-e053-2995a90a54642025-09-18WarningsExact identifier
spl set id: c69f07b1-660a-db03-e053-2995a90a5464

Reported adverse events (FAERS/openFDA)#

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