PHOSPHORUS

Manufacturer: STANDARD HOMEOPATHIC COMAPNY
Effective date: 2021-12-06
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: legacy-cache
Hydrated at: 2026-08-01 22:24:33

Label at a glance#

ProductPHOSPHORUS

Active ingredientPHOSPHORUS

Label structure8 sections

Dosage and administration

Adults: Dissolve 4 tablets under tongue 4 times a day. Children: Consult a healthcare professional

Contacts and useful links#

PhoneLabel contact800-624-9659

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Made according to the
Homeopathic Pharmacopoeia
of the United States since 1903.

Warnings

WARNINGS SECTION

Do not use if cap band is missing or broken.

If you are pregnant or nursing, consult a licensed health care professional before using this product.

If symptoms persist for 7 days or worsen, contact a licensed practitioner.

To be used according to label indications and/or standard homeopathic indications

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all medicines out of the reach of children.

OTC - QUESTIONS SECTION

Standard Homeopathic Company
Los Angeles, CA 90061
Questions? 800-624-9659

Directions

DOSAGE & ADMINISTRATION SECTION

Adults: Dissolve 4 tablets under tongue 4 times a day.
Children: Consult a healthcare professional

INACTIVE INGREDIENT SECTION

In a base of Acacia Gum and Lactose N.F.

OTC - ACTIVE INGREDIENT SECTION

PHOSPHORUS 6X

INDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

COUGH OR CHEST CONGESTION

Principal Display Panel -- 250 Tablet Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Standard

Homeopathic

Made in the USA Since 1903

NDC # 0360-0305-01

Homeopathic Medicine

PHOSPHORUS

COUGH OR CHEST

CONGESTION*

*Claims based on traditional homeopathic

practice, not accepted medical evidence.

Not FDA evaluated.

250 TABLETS

label

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

PHOSPHORUS
LACTOSE MONOHYDRATE
ACACIA

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
0360-0305	0360-0305-01

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
Name	UNII	Kind
LACTOSE MONOHYDRATE	EWQ57Q8I5X	IACT
ACACIA	5C5403N26O	IACT
PHOSPHORUS	27YLU75U4W	ACTIB

Source Document#

Source XML · Source PDF

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
d27f21aa-2a18-54b5-e053-2995a90ae549			4da00cd5-959c-512d-e054-00144ff88e88	2021-12-06	Warnings	Exact identifier spl id: d27f21aa-2a18-54b5-e053-2995a90ae549 spl set id: 4da00cd5-959c-512d-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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