CHLAMYDIA REMEDY- chlamydia trachomatis liquid
Deseret Biologicals, Inc.

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:

Chlamydia Trachomatis 12X, 15X, 20X, 30X, 60X, 120X, 150X, 200X, 500X, 1000X.

INDICATIONS:

For temporary relief of symptoms related to chlamydia infections. Male: burning sensation during urination, discharge from penis, testicular tenderness or pain and rectal discharge or pain. Female: vaginal discharge, burning sensation during urination, painful sexual intercourse, rectal pain or discharge, liver pain, dark colored urine and clay colored feces.

WARNINGS:

Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away.

If pregnant or breast-feeding, ask a health professional before use.

Tamper seal: "Sealed for Your Protection." Do not use if seal is broken or missing.

KEEP OUT OF REACH OF CHILDREN:

Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away.

DIRECTIONS:

1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

INDICATIONS:

INACTIVE INGREDIENTS:

Demineralized Water, 25% Ethanol

QUESTIONS:

Dist. By: Deseret Biologicals, Inc.

469 W. Parkland Drive

Sandy, UT 84070 www.desbio.com

PACKING LABEL DISPLAY:

DESBIO

NDC 43742-0500-1

HOMEOPATHIC

CHLAMYDIA REMEDY

1 FL OZ (30 ml)

Chlamydia Remedy

CHLAMYDIA REMEDY
chlamydia trachomatis liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:43742-0500
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CHLAMYDIA TRACHOMATIS (UNII: T6NI39QU44) (CHLAMYDIA TRACHOMATIS - UNII:T6NI39QU44)	CHLAMYDIA TRACHOMATIS	12 [hp_X] in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:43742-0500-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	09/10/2014	09/28/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		09/10/2014	09/28/2020

Labeler - Deseret Biologicals, Inc. (940741853)

Registrant - Apotheca Company (844330915)

Name	Address	ID/FEI	Business Operations
Establishment
Apotheca Company		844330915	manufacture(43742-0500) , api manufacture(43742-0500) , label(43742-0500) , pack(43742-0500)

Revised: 4/2018

Document Id: a76401bc-1a09-44b5-b42b-5a5953ee2734

Set id: e6b6fb5c-6dde-4243-971a-5a8ab5e0e5a3

Version: 3

Effective Time: 20180419

Deseret Biologicals, Inc.