Antacid Strawberry Relief Chews

Manufacturer
Target Corporation | Bestco Inc.
Effective date
2018-01-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:04:00

Label at a glance#

ProductAntacid Strawberry Relief Chews
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

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 - WHEN USING SECTION

Do not take more than 5 chewable tablets in a 24-hour period, or use the maximum dosage for more than 2 weeks, except under the advice and supervision of a physician.

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 300 mg, magnesium 1 mg

Contains soy

INACTIVE INGREDIENT SECTION

Inactive ingredients: Beeswax, carmine, carnauba wax, citric acid, corn starch, corn syrup, ethyl acetate, FD&C blue no. 1 aluminum lake, FD&C red no. 40 aluminum lake, FD&C yellow no. 6 aluminum lake, gum arabic, hydrogenated coconut oil, maltodextrin, medium chain triglycerides, modified corn starch, natural and artificial flavors, phosphoric acid, pregelatinized corn starch, propylene glycol, purified water, shellac, sodium benzoate, sorbic acid, sorbitol, soy lecithin, soybean oil, sucrose and titanium dioxide.

OTC - QUESTIONS SECTION

Questions? Or to report an adverse event call 1-800-910-6874

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Target Antacid Berry Bites 32ctTarget Antacid Berry Bites 32ct

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
11673-042-322022-07-05C16284748780-19d75b9d0-ec53-f424-e053-dadaa90a57ceCalcium Carbonate 750 mg
11673-042-322020-01-31C16284748780-19d75b9d0-ec53-f424-e053-dadaa90a57ceCalcium Carbonate 750 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
11673-04211673-042-32

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
e312ff7c-9ccb-7cf0-e053-2995a90af28263f05c14-a973-7ca7-e053-2a91aa0a8f1a2022-07-05WarningsExact identifier
spl set id: 63f05c14-a973-7ca7-e053-2a91aa0a8f1a

Reported adverse events (FAERS/openFDA)#

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