LIFE Q- sodium bicarbonate tablet

LIFE Q by

Drug Labeling and Warnings

LIFE Q by is a Otc medication manufactured, distributed, or labeled by Saenggi Life. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient[s]

Sodium bicarbonate 60%

Purpose

Hand Sanitizer

Use[s]

Virus, bacteria, bacteria removal and infection prevention effect from all spaces and objects in daily life.

Recommended for repeated use.

Warinings

For external use only. Flammable. Keep away from geat or flame

Do not use

• Do not eat.
• Do not spray directly on the body.

When using this product

keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

In case of adverse skin reactions

visit a hospital and follow your doctor's instructions.

Keep out of reach of children.

Directions

• Put 1 tablet of disinfectant in 2 liters of water and wait for 2 minutes.
• Put it in a sprayer and spray an appropriate amount on the area where virus, bacteria, and bacteria need to be sterilized.
• It is recommended to use 1 tablet of disinfectant in an electric sprayer with a capacity of 2L to 3L.

Other information

• Sealed storage lengthens the storage period.
• Avoid direct sunlight and store in a cool dry place.

Inactive ingredients

Sodium chlorite, Sodium sulfite, Citric acid, Maleic acid

Package Label

INGREDIENTS AND APPEARANCE

LIFE Q 
sodium bicarbonate tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80760-201
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO) (BICARBONATE ION - UNII:HN1ZRA3Q20)	SODIUM BICARBONATE	60 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORITE (UNII: G538EBV4VF)
SODIUM SULFITE (UNII: VTK01UQK3G)
MALEIC ACID (UNII: 91XW058U2C)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	12mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80760-201-01	20 g in 1 BOTTLE; Type 0: Not a Combination Product	10/12/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		10/12/2020

Labeler - Saenggi Life (695012496)

Registrant - Saenggi Life (695012496)

Establishment
Name	Address	ID/FEI	Business Operations
Saenggi Life		695012496	manufacture(80760-201)