FDA.reportPublic FDA data

Inflammation

Manufacturer
Deseret Biologicals, Inc. | Apotheca Company
Effective date
2016-10-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:22:23

Label at a glance#

ProductInflammation II
Active ingredientASAFETIDA, KALMIA LATIFOLIA LEAF, CAUSTICUM, COLCHICUM AUTUMNALE BULB, IRON, PSEUDOGNAPHALIUM OBTUSIFOLIUM, LITHIUM BENZOATE, MERCURIC OXIDE, TOXICODENDRON PUBESCENS LEAF, FILIPENDULA ULMARIA ROOT
Label structure9 sections

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

Asafoetida 8X, Kalmia Latifolia 8X, Causticum 10X, Colchicum Autumnale 10X, Ferrum Metallicum 10X, Gnaphalium Polycephalum 10X, Lithium Benzoicum 10X, Mercurius Praecipitatus Ruber, Rhus Tox 10X, Spiraea Ulmaria 10X.

HOMEOPATHIC INDICATIONS:

OTC - PURPOSE SECTION

For temporary relief of pain, stiffness, inflammation, and conditions of the tendons and ligaments; backache, shoulder and arm pain, joint pain.**

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

WARNINGS:

WARNINGS SECTION

Keep out of reach of children. In case of overdose, contact physician or Poison Control Center right away.

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

Tamper seal: "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

Keep out of reach of children. In case of overdose, contact 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.

HOMEOPATHIC INDICATIONS:

INDICATIONS & USAGE SECTION

For temporary relief of pain, stiffness, inflammation, and conditions of the tendons and ligaments; backache, shoulder and arm pain, joint pain.**

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

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

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DESBIO

NDC 43742-0744-1

HOMEOPATHIC

INFLAMMATION II

1 FL OZ (30 ml)

Inflammation IIInflammation II

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43742-074443742-0744-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
ASAFETIDAW9FZA51AS1ACTIB
KALMIA LATIFOLIA LEAF79N6542N18ACTIB
CAUSTICUMDD5FO1WKFUACTIB
COLCHICUM AUTUMNALE BULB993QHL78E6ACTIB
IRONE1UOL152H7ACTIB
PSEUDOGNAPHALIUM OBTUSIFOLIUM36XQ854NWWACTIB
LITHIUM BENZOATER9Z042Z19EACTIB
MERCURIC OXIDEIY191986AOACTIB
TOXICODENDRON PUBESCENS LEAF6IO182RP7AACTIB
FILIPENDULA ULMARIA ROOT997724QNDSACTIB
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
d180d8ad-5d16-4d3c-a826-f5925e4129dbf9909e30-9c58-4f50-88f5-be145c8d82322016-10-14WarningsExact identifier
spl id: d180d8ad-5d16-4d3c-a826-f5925e4129db
spl set id: f9909e30-9c58-4f50-88f5-be145c8d8232

Reported adverse events (FAERS/openFDA)#

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