KI NO SIN- calcium carbonate capsule

Ki No Sin by

Drug Labeling and Warnings

Ki No Sin by is a Otc medication manufactured, distributed, or labeled by NPG Bio Pharmaceuticals Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Calcium Carbonate (CaCO3) 5.5%, 55 mg

Purposes

Promotes overall health and wellness for those managing diabetes and kidney conditions by providing essential support. Helps to regulate and normalize the body’s critical signaling processes for improved physiological function.

Uses

This health supplement can be used to aid in the improvement of body functions compromised by diabetes and kidney disease, and to help maintain normal calcium ion levels.

Warnings

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

Consult a healthcare professional before use if you are pregnant or breastfeeding.

Do not exceed the recommended dosage.

Swallow with sufficient water or a beverage to prevent aspiration.

Warnings

Keep out of reach of children

Pregnant women are advised to consult with their healthcare provider prior to use.

Warnings

Stop use and ask a doctor if

symptoms persist or get worse.

Warnings

When using this product

do not use more than directed.

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

Warnings

Ensure that the included desiccant is not ingested.

Directions

Adults and teenagers (18+ years): Take 2 tablets 2-3 times daily.

Children aged 12-18 years: Take 1 tablet once daily.

Inactive Ingredients

Microcrystalline Cellulose, Chitosan, lactose, Gardenia Florida Fruit Extract, Gardenia Jasminoides Fruit Extract, Magnesium Oxide, Maltodextrin, Vitis Vinifera (Grape) Juice Powder, Hydroxypropyl Methylcellulose, Flavor, Cyanocobalamin, Magnesium Stearate, Cholecalciferol, Zinc Oxide, Glucosamine Hydrochloride, Ginkgo Biloba Leaf Extract, Nelumbo Nucifera (Lotus) Leaf Powder, Silk Extract

Label

INGREDIENTS AND APPEARANCE

KI NO SIN 
calcium carbonate capsule

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84540-323
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB)	CALCIUM CARBONATE	55 mg  in 500 mg

Inactive Ingredients
Ingredient Name	Strength
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)
HYPROMELLOSES (UNII: 3NXW29V3WO)
ZINC OXIDE (UNII: SOI2LOH54Z)
WINE GRAPE JUICE (UNII: JHQ6158A7R)
GARDENIA JASMINOIDES FRUIT (UNII: 7CTH8MD549)
CHOLECALCIFEROL (UNII: 1C6V77QF41)
MAGNESIUM STEARATE (UNII: 70097M6I30)
GLUCOSAMINE HYDROCHLORIDE (UNII: 750W5330FY)
GINKGO (UNII: 19FUJ2C58T)
BOMBYX MORI FIBER (UNII: 6LK42KUV6W)
NELUMBO NUCIFERA LEAF (UNII: 60C608DPVT)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
MAGNESIUM OXIDE (UNII: 3A3U0GI71G)
POLIGLUSAM (UNII: 82LKS4QV2Y)
CYANOCOBALAMIN (UNII: P6YC3EG204)

Product Characteristics
Color	white	Score	no score
Shape	CAPSULE	Size	10mm
Flavor	GRAPE	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84540-323-01	500 mg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/29/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M022	08/29/2024

Labeler - NPG Bio Pharmaceuticals Co.,Ltd. (963309698)