SEYIP- calcium carbonate liquid

SEYIP by

Drug Labeling and Warnings

SEYIP by is a Otc medication manufactured, distributed, or labeled by seaip co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

calcium carbonate

Purpose

Antimicrobial

Use

1. Try to mix with eggbeater before building

2. Possibly using wall, roof etc. when it process hardened

Use

3. Must spread two times after go by 30 minutes firstly

4. Have to construct using high pressure airless

Warnings

Do not melt with liquid paint

Do not construct rainy( more than 85%) and hard frost(lesser than 5°C) days

Using quickly possibly because it is rancid when long term storage

Keep a frigid place and avoid direct sunlight

Warnings

Flammable, Keep away from flame, keep out of eyes. In case of eye contact immediately flush eyes with water then contact physician.

Warnings

Keep out of reach of children

Inactive Ingredient

POLYQUATERNIUM-10 (1000 MPA.S AT 2%)

4-METHYL-1-PENTANOL

CALCIUM HYDROXIDE

ZEOLITE A

WATER

ALUMINUM SILICATE

SODIUM ALGINATE

KAOLIN

SODIUM BIS(1,3-DIMETHYLBUTYL) SULFOSUCCINATE

DIATOMACEOUS EARTH

Package Label

syeip image

INGREDIENTS AND APPEARANCE

SEYIP 
calcium carbonate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82585-303
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB)	CALCIUM CARBONATE	3 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
DIATOMACEOUS EARTH (UNII: 2RF6EJ0M85)
WATER (UNII: 059QF0KO0R)
POLYQUATERNIUM-10 (1000 MPA.S AT 2%) (UNII: GMR4PEN8PK)
ALUMINUM SILICATE (UNII: T1FAD4SS2M)
SODIUM ALGINATE (UNII: C269C4G2ZQ)
KAOLIN (UNII: 24H4NWX5CO)
SODIUM BIS(1,3-DIMETHYLBUTYL) SULFOSUCCINATE (UNII: AA05A04D8O)
4-METHYL-1-PENTANOL (UNII: X796XFP7D4)
CALCIUM HYDROXIDE (UNII: PF5DZW74VN)
ZEOLITE A (UNII: Y3NG9WF08W)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82585-303-01	500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/06/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		03/06/2022

Labeler - Seaip co., Ltd (694211270)

Registrant - Seaip co., Ltd (694211270)