Drugplain

RockHomo 10 [hp_C]/mL

Rickettsia Nosode (Rickettsia Prowazekii) · LIQUID · Deseret Biologicals, Inc.

No Recall History
Plain English

RockHomo is a liquid containing rickettsia nosode (rickettsia prowazekii) at 10 [hp_C]/mL, taken oral. Manufactured by Deseret Biologicals, Inc..

Key Facts

Brand Name
RockHomo
Generic Name
Rickettsia Nosode (Rickettsia Prowazekii)
NDC Code (Product)
43742-1972
Manufacturer
Deseret Biologicals, Inc.
Strength
10 [hp_C]/mL
Dosage Form
LIQUID
Route
ORAL
Marketing Status
Marketing Start
09/17/2020

Recall History

No Recall History

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

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 & Administration

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.

Warnings

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.

Frequently Asked Questions

What is RockHomo used for?

RockHomo contains Rickettsia Nosode (Rickettsia Prowazekii). It is a liquid taken oral. Consult your doctor for specific uses.

Is RockHomo a controlled substance?

RockHomo is not classified as a controlled substance by the DEA.

What is the generic name for RockHomo?

The generic name for RockHomo is Rickettsia Nosode (Rickettsia Prowazekii). There are no other listed brand versions of Rickettsia Nosode (Rickettsia Prowazekii).

What is the NDC code for RockHomo 10 [hp_C]/mL?

The NDC (National Drug Code) for RockHomo 10 [hp_C]/mL is 43742-1972, listed by Deseret Biologicals, Inc..

Product NDC

43742-1972

Package NDC

43742-1972-1

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)