OHM FLU

Manufacturer
OHM PHARMA INC.
Effective date
2021-12-29
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:15:30

Label at a glance#

ProductOHM FLU
Active ingredientCAIRINA MOSCHATA HEART/LIVER AUTOLYSATE, INFLUENZA A VIRUS, INFLUENZA B VIRUS
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS (HPUS*): Equal amounts of: Anas barbariae, hepatis et cordis extractum 200C, Influenzinum 9C.

OTC - ACTIVE INGREDIENT SECTION

*The letters "HPUS" indicate the components in this product are officially monographed in the Homeopathic Pharmacopeia of the United States.

INDICATIONS & USAGE SECTION

USES: Temporarily relieves relieves fever, congestion, body aches and pains. To help reduce and prevent the development of flu symptoms.**

SPL UNCLASSIFIED SECTION

**This statement has not been evaluated by the FDA.
It is based on documented Homeopathic Materia Medica.

WARNINGS SECTION

WARNINGS:

IF PREGNANT OR BREAST-FEEDING, ask a health professional before use. If symptoms persist for more than 3 days, discontinue use and contact a health professional.

This product is not intended to be an alternative to vaccination.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF THE REACH OF CHILDREN.

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS: To open ampoule snap top up and away from you. Using pipette place entire content under the tongue, hold it for 30 seconds and swallow.

FLU PREVENTION PROTOCAL: Adults and children over 6 years: Take 1 ampoule every week for six weeks. FLU TREATMENT PROTOCOL: Take 1 dose at the first sign of flu or 1 dose every 12 hours according to symptoms. Children under 6 years old: use half the adult dose. Children under 2: consult a health professional before use.

Discard unused solution. Solution does not contain any preservatives.

Not for injection.

OTHER SAFETY INFORMATION

OTHER INFORMATION: Store at controlled room temperature. Tamper evident seal. Do not use if box seal is missing or broken.

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: Isotonic sodium chloride solution.

OTC - QUESTIONS SECTION

Mfg. By: OHM PHARMA, INC. / Mineral Wells, TX 76067

Made in USA

www.ohmpharma.com

OTC - PURPOSE SECTION

Flu, fever, congestion, body aches and pains relief

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 66096-170-06

OHM FLU

HOMEOPATHIC MEDICINE

Pharmaceutical Grade. Professional use only.

CONTENTS: 12 oral ampoules of 2.2 ml each.

Terrain Box EnglishTerrain Box English

Terrain Box SpanishTerrain Box Spanish

Ampoule BoxAmpoule Box

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Insert SpanishInsert Spanish

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66096-170-06OHM FLU12 in 1 BOXLIQUID124
66096-170-06OHM FLU2.2 mL in 1 AMPULELIQUID2.24

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66096-170OHM FLU (ANAS BARBARIAE, HEPATIS ET CORDIS EXTRACTUM, INFLUENZINUM) LIQUID [OHM PHARMA INC.]4Current NDC, Legacy NDC, 2 package rows20211230_e5804d17-5ff8-459d-9b94-de2134930201.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66096-17066096-170-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

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
OHM FLUANAS BARBARIAE, HEPATIS ET CORDIS EXTRACTUM, INFLUENZINUMOHM PHARMA INC.e5804d17-5ff8-459d-9b94-de21349302012021-12-29WarningsExact identifier
ndc (package): 66096-170-06
ndc (product): 66096-170
ndc11 (package): 66096017006
spl id: d44b1652-5ba4-2927-e053-2a95a90a48f9
spl set id: e5804d17-5ff8-459d-9b94-de2134930201

Reported adverse events (FAERS/openFDA)#

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