HERZ HOMO- herpes zoster nosode 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:

Herpes Zoster Nosode 15X, 20X, 30X, 60X, 90X, 120X, 150X, 200X, 500X, 1000X.

PURPOSE:

Herpes Zoster Nosode - Itching, Tingling, Painful Rash of Body, Rash on Side of Face, Painful Rash on Face

USES:

• For the temporary relief of symptoms including:

• itching • tingling • painful rash of body

• rash on side of face • painful rash on face

These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

WARNINGS:

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

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

Tamper Evident: Sealed for your protection. Do not use if seal is broken or missing.

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.

INACTIVE INGREDIENTS:

Demineralized water, 25% ethanol

QUESTIONS:

Dist. By: Deseret Biologicals, Inc.

469 W. Parkland Drive

Sandy, UT 84070

www.desbio.com

800-827-8204

PACKAGE LABEL DISPLAY:

DesBio

HERZ:HOMO

Homeopathic

NDC 43742-1889-1

1 FL OZ (30 ml)

HERZ:HOMO

HERZ HOMO 
herpes zoster nosode liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43742-1889
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HUMAN HERPESVIRUS 3 (UNII: 9885M7D6JP) (HUMAN HERPESVIRUS 3 - UNII:9885M7D6JP) HUMAN HERPESVIRUS 315 [hp_X]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:43742-1889-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product09/23/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic09/23/2020
Labeler - Deseret Biologicals, Inc. (940741853)
Registrant - Apotheca Company (844330915)
Establishment
NameAddressID/FEIBusiness Operations
Apotheca Company844330915manufacture(43742-1889) , api manufacture(43742-1889) , label(43742-1889) , pack(43742-1889)

Revised: 3/2024
 
Deseret Biologicals, Inc.