CERAVIDA FRESH- chitosan liquid

CERAVIDA FRESH by

Drug Labeling and Warnings

CERAVIDA FRESH by is a Otc medication manufactured, distributed, or labeled by G.CLO CO., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Chitosan 5%

Purpose

Anti-Odor

Uses

Anti-odor treatment agents for all Textiles to prevents and removes odor molecules and microbes.

Inactive Ingredients

Acetic acid, Water

Warnings

Eyes

Immediately flush eyes with plenty of water. Contact a physician.

Skin Inhalation

In case of skin contact, the compound is not Hazardous, but cleansing the skin after use is advisable.

Prolonged inhalation of vapors can cause irritation to respiratory system. If prolonged inhalation is necessary use an approved NIOSH/MSHA respirator.

Keep out of reach of children

If swallowed, get medical help or contact a physician.

Directions How to use

- Mix together in the proper proportion with the water in the tenter's water bath.

- Ceravida Fresh dosage is different depending on the tenter capacity.

- It must be sufficiently mixed with the water at a rate of about 5-10% dosage to process the fabric.

How to keep

It is recommended to store at room temperature where sunlight does not reach directly and in closed containers. The viscosity may increase during long-term storage, resulting in sediment. It is directly soluble in water.

Package Label

INGREDIENTS AND APPEARANCE

CERAVIDA FRESH 
chitosan liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78543-100
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POLIGLUSAM (UNII: 82LKS4QV2Y) (POLIGLUSAM - UNII:82LKS4QV2Y)	POLIGLUSAM	5 kg  in 100 kg

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ACETIC ACID (UNII: Q40Q9N063P)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78543-100-11	10 kg in 1 BOTTLE; Type 0: Not a Combination Product	06/02/2020
2	NDC: 78543-100-22	20 kg in 1 BOTTLE; Type 0: Not a Combination Product	06/02/2020
3	NDC: 78543-100-33	50 kg in 1 BOTTLE; Type 0: Not a Combination Product	06/02/2020
4	NDC: 78543-100-44	100 kg in 1 BOTTLE; Type 0: Not a Combination Product	06/02/2020
5	NDC: 78543-100-55	1000 kg in 1 BOTTLE; Type 0: Not a Combination Product	06/02/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		06/02/2020

Labeler - G.CLO CO., LTD (690058546)

Registrant - G.CLO CO., LTD (690058546)

Establishment
Name	Address	ID/FEI	Business Operations
G.CLO CO., LTD		690058546	manufacture(78543-100)