DRUG FACTS

Drug Labeling and Warnings

Drug Details [pdf]

TOTAL CHLORINE- chlorinum liquid 
White Manufacturing Incorporated DBA Micro-West

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

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DRUG FACTS

Active Ingredients

Chlorinum 15X, 30X, 200C, 1M

Uses

apathy, cold, convulsions, upper respiratory homeostasis, impotence, spasms of the throat, lung membrane inflammation, sore throat, ulcers, spasms, apprehension, irritability, dry mouth, irritability to swallow

Keep Out of Reach of Children

KEEP OUT OF REACH OF CHILDREN

INDICATIONS

Indications: apathy, cold, convulsions, upper respiratory homeostasis, impotence, spasms of the throat, lung membrane inflammation, sore throat, ulcers, spasms, apprehension, irritability, dry mouth, irritability to swallow

WARNINGS

Warning:

STOP USE AND CALL A DOCTOR if symptoms persist or worsen. IF PREGNANT OR BREAST FEEDING, consult a healthcare professional before use. CONTAINS ALCOHOL: in case of accidental overdose, consult a poison control center immediately.

Other safety information: Tamper resistant for your protection. Use only if safety seal is intact

Directions

Take 6 drops, 4 times a day, For ages 2 to adult

Alcohol (20% v/v)

Purified water

TOTAL CHLORINE 
chlorinum liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 61657-0973
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Chlorine (UNII: 4R7X1O2820) (Chlorine - UNII:4R7X1O2820)	Chlorine	15 [hp_X]  in 30 mL

Inactive Ingredients
Ingredient Name	Strength
Alcohol (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 61657-0973-1	30 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	08/20/2019	08/20/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		08/15/2011	08/20/2019

Labeler - White Manufacturing Incorporated DBA Micro-West (082307831)

Establishment
Name	Address	ID/FEI	Business Operations
King Bio Inc		617901350	manufacture(61657-0973) , pack(61657-0973) , label(61657-0973)

Revised: 8/2019

Document Id: 4adc3307-ac51-42f4-b929-32a538f18578

34390-5

Set id: db4c11cf-649b-4cbb-ae99-efb213d17119

Version: 7

Effective Time: 20190820

 

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