OTC Medication Information: AI Kungang

AI KUNGANG- calcium carbonate liquid
TheJoenSpace Co,. LTD

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

calcium carbonate

Carboxymethyl cellulose sodium salt, guargum, water

40% reduction in radon
TVOC reduction
Reduction of formaldehyde
Toluene reduction
More than 99% antibacterial
More than 80% of deodorization
Moisture absorption/moisture proof
No heavy metal detection
Firefighting: Semi-incombustible
Radiation of 90.2% of far-infrared rays

■ if following abnormal symptoms persist, discontinue use

Irritation around the eyes, ears, mucous membranes, including the mouth, under the skin irritation and rashes

■ Stop immediately and consult a doctor if you experience

1) Hypersensitivity symptoms such as erythema, itching and dermatitis.

2) Skin Irritation

3) Following Instructions when using medication

(1) For external use only (Do not use internally)

(2) Avoid getting into the eyes (if contact occurs, wash well with clean water)

■ Be careful not to inhale or use excessively for a long time (ingesting ethanol repeatedly causes irritation to mucous membranes and headaches or other symptoms may appear. When used repeatedly in the same area, skin irritation may occur.

■ Do not use the product for a long time in the same area as swelling, inflammation or sickness may occur due to absorption through the skin.

It is not recommended to use this one areas that have been medically treated with a cast or bandage.

■ Do not use in combination with soap or antibacterial cleansing agents.

• Keep Out of Reach of Children.

■ apply proper amount to the skin

for external use only

label
(click image for full-size original)

AI KUNGANG
calcium carbonate liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:81768-0001
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CALCIUM CARBONATE (CALCIUM CATION) CALCIUM CARBONATE 55 g in 100 mL
Inactive Ingredients
Ingredient Name Strength
WATER
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:81768-0001-1 2000 mL in 1 CAN None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 04/14/2021
Labeler — TheJoenSpace Co,. LTD (695644078)
Registrant — TheJoenSpace Co,. LTD (695644078)
Establishment
Name Address ID/FEI Operations
TheJoenSpace Co,. LTD 695644078 manufacture (81768-0001)

Revised: 04/2021 TheJoenSpace Co,. LTD

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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