Alpha CF Cold and Flu Tablets

Manufacturer
Schwabe North America, Inc. | Schwabe Mexico, S.A. de C.V.
Effective date
2022-03-21
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 22:05:17

Label at a glance#

ProductALPHA CF
Active ingredientACONITUM NAPELLUS, BRYONIA ALBA ROOT, EUPATORIUM PERFOLIATUM FLOWERING TOP, GELSEMIUM SEMPERVIRENS ROOT, IPECAC, EUCALYPTUS GLOBULUS LEAF, PHOSPHORUS
Label structure12 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Aconitum napellus 4X

Bryonia 4X

Eupatorium perfoliatum 6X

Gelsemium sempervirens 4X

Ipecacuanha 3X

Phosphorus 6X

Eucalyptus globulus 2X

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Cellulose

Lactose monohydrate

Magnesium stearate

Dosage & Administration

DOSAGE & ADMINISTRATION SECTION

Directions: Sublingual medication. Place tablet under tongue and let dissolve slowly.

Best if taken at least 15 minutes before and a half hour after eating, brushing teeth, or drinking anything except water.

Adults and children 12 years of age and older: At first sign of cold or flu, take 1 tablet every hour and 2 or 3 tablets before going to sleep.

As symptoms subside, take 1 tablet every 2 or 3 hours.


Children 6 to 12: Take 1/2 tablet every hour and 1 or 1 1/2 tablets before going to sleep.

As symptoms subside, take 1/2 tablet every 2 or 3 hours.


Children under 6: Consult a physician.

Indication & Usage

INDICATIONS & USAGE SECTION

Temporarily relieves these symptoms: fever, chills, sneezing, stuffed-up nose, runny nose, coughing, sore throat, headache, minor aches and pains.

Purpose

OTC - PURPOSE SECTION

Temporarily relieves these symptoms: fever, chills, sneezing, stuffed-up nose, runny nose, coughing, sore throat, headache, minor aches and pains.

Warnings

WARNINGS SECTION

Sore Throat Warning: severe or persistent sore throat for more that 2 days or if accompanied by high fever, headache, nausea, vomiting or rash may be serious.

Consult a physician promptly.

Ask Doctor

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have a persistent or chronic cough that lasts, is chronic such as occurs with smoking, asthma, chronic bronchitis, or emphysema or is accompanied by excessive phlegm (mucus).

Stop Use

OTC - STOP USE SECTION

Stop use and ask a doctor if new symptoms occur, symptoms worsen or do not get better within 7 days, fever worsens or lasts more than 3 days, cough lasts more than 7 days or occurs with rash or persisitent headache.
These could be signs of a serious condition.

Pregnancy or Breast Feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children.

Overdosage

OVERDOSAGE SECTION

In case of overdose, seek medical help or contact a Poison Control Center immediately.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Alpha CF_06.jpgAlpha CF_06.jpg

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53499-9490ALPHA CF (ACONITUM NAPELLUS, BRYONIA ALBA ROOT, EUCALYPTUS GLOBULUS LEAF, EUPATORIUM PERFOLIATUM FLOWERING TOP, GELSEMIUM SEMPERVIRENS ROOT, IPECAC, PHOSPHORUS) TABLET [SCHWABE NORTH AMERICA, INC.]6Legacy NDC20220323_4ae6b570-5924-485b-b8dc-b79ab8d42f44.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
53499-949053499-9490-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
72b5f627-4426-4fe0-9ebe-caec26fce1f94ae6b570-5924-485b-b8dc-b79ab8d42f442022-03-21WarningsExact identifier
spl id: 72b5f627-4426-4fe0-9ebe-caec26fce1f9
spl set id: 4ae6b570-5924-485b-b8dc-b79ab8d42f44

Reported adverse events (FAERS/openFDA)#

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