FDA.reportPublic FDA data

Co De R T

Manufacturer
QN SCIENCE Co Ltd
Effective date
2022-10-24
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 21:51:01

Label at a glance#

ProductCo De R T
Active ingredientCALCIUM CARBONATE
Label structure11 sections

Dosage and administration

Adults and children 18 years and over take 3 tablets 2~3 times a day Children 12 to 18 years take 1~2 tablets 2 times a day Children 8 to 12 years take 1/2 tablets 2 times a day

Label contents#

Full prescribing information#

active ingredients

OTC - ACTIVE INGREDIENT SECTION

Shell powder (CaCo3) 0.45%

purpose

OTC - PURPOSE SECTION

relieves symptoms from Covid-19 or various infection.

Pain reliever / fever reducer / Nasal decongestant

use

INDICATIONS & USAGE SECTION

Covid-19 treatment supplements without side effects

Warnings

OTC - DO NOT USE SECTION

if you are allergic to any of the ingredients in this product.

Warnings

OTC - WHEN USING SECTION

■ do not use more than directed.

■ take with enough water or drink to avoid getting into airway.

Warnings

OTC - STOP USE SECTION

new symptoms occur or symptoms worsen

Warnings

WARNINGS SECTION

Be careful not to take the included desiccant.

Warnings

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If pregnant or breast-feeding, ask a health professional before use.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 18 years and over

take 3 tablets 2~3 times a day

Children 12 to 18 years

take 1~2 tablets 2 times a day

Children 8 to 12 years

take 1/2 tablets 2 times a day

inactive ingredients

INACTIVE INGREDIENT SECTION

Magnesium oxide, Gryllus bimaculatus, Shiitake mushroom,

Mulberry Leaf, Vitamin C, Microcrystalline Cellulose, Carboxymethyl cellulose, Silanedione, Magnesium Stearate

label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Co Re D T LabelCo Re D T Label82932-302

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82932-30282932-302-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
SHIITAKE MUSHROOM1A64QN2D2FIACT
ASCORBIC ACIDPQ6CK8PD0RIACT
CARBOXYMETHYLCELLULOSE05JZI7B19XIACT
SILANDRONEYY7GL3CCE9IACT
MAGNESIUM STEARATE70097M6I30IACT
MORUS ALBA LEAFM8YIA49Q2PIACT
MAGNESIUM OXIDE3A3U0GI71GIACT
GRYLLUS BIMACULATUS5JRP32U52AIACT
CELLULOSE, MICROCRYSTALLINEOP1R32D61UIACT
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
ebc3ad65-5814-e025-e053-2a95a90afe9ee83bc698-60ce-1a84-e053-2995a90a56812022-10-24WarningsExact identifier
spl id: ebc3ad65-5814-e025-e053-2a95a90afe9e
spl set id: e83bc698-60ce-1a84-e053-2995a90a5681

Reported adverse events (FAERS/openFDA)#

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