RockHomo

Manufacturer
Deseret Biologicals, Inc. | Apotheca Company
Effective date
2024-02-26
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 02:26:10

Label at a glance#

ProductRockHomo
Active ingredientRICKETTSIA PROWAZEKII
Label structure9 sections

Indications and uses

• For the temporary relief of symptoms including: • Rash • Fever • Nausea • Muscle Pain • Lack of Appetite • Abdominal Pain  • Joint Pain • Occasional Diarrhea These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Dosage and administration

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.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Rickettsia Nosode (Rickettsia Prowazekii) 10C, 12C, 15C, 30C, 45C, 60C, 75C, 100C, 250C, 500C. 

PURPOSE:

OTC - PURPOSE SECTION

Rickettsia Nosode (Rickettsia Prowazekii) - Rash, Fever, Nausea, Muscle Pain, Lack of Appetite, Abdominal Pain, Joint Pain, Occasional Diarrhea

USES:

INDICATIONS & USAGE SECTION

• For the temporary relief of symptoms including:

• Rash • Fever • Nausea • Muscle Pain

• Lack of Appetite • Abdominal Pain 

• Joint Pain • Occasional Diarrhea

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

WARNINGS:

WARNINGS SECTION

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:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of overdose, contact a physician or Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

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:

INACTIVE INGREDIENT SECTION

Demineralized water, 25% ethanol

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. By: Deseret Biologicals, Inc.
469 W. Parkland Drive
Sandy, UT 84070

www.desbio.com

800-827-8204

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DesBio

ROCK:HOMO

Homeopathic

NDC 43742-1972-1

1 FL OZ (30 ml)

Rock:HomoRock:Homo

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43742-1972-1RockHomo30 mL in 1 BOTTLE, DROPPERLIQUID305

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43742-1972ROCKHOMO (RICKETTSIA NOSODE (RICKETTSIA PROWAZEKII)) LIQUID [DESERET BIOLOGICALS, INC.]5Current NDC, Legacy NDC, 1 package rows20240228_fefea641-ab32-48b6-87e3-39e20628228c.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43742-197243742-1972-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
RICKETTSIA PROWAZEKIITVS414L9M5ACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
RockHomoRICKETTSIA NOSODE (RICKETTSIA PROWAZEKII)Deseret Biologicals, Inc.fefea641-ab32-48b6-87e3-39e20628228c2024-02-26WarningsExact identifier
ndc (package): 43742-1972-1
ndc (product): 43742-1972
ndc11 (package): 43742197201
spl id: 92ccb097-92a6-4189-b81d-6c26ad866b6e
spl set id: fefea641-ab32-48b6-87e3-39e20628228c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.