Injury

Manufacturer
Natural Creations, Inc | OHM Pharma, Inc
Effective date
2025-12-16
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:36:00

Label at a glance#

ProductInjury
Active ingredientCALENDULA OFFICINALIS FLOWERING TOP, COMFREY ROOT, ARNICA MONTANA WHOLE, BELLIS PERENNIS WHOLE, BRYONIA ALBA ROOT, HYPERICUM PERFORATUM WHOLE, RHODODENDRON TOMENTOSUM LEAFY TWIG, PHOSPHORUS, TOXICODENDRON PUBESCENS LEAF, RUTA GRAVEOLENS FLOWERING TOP, DELPHINIUM STAPHISAGRIA SEED, RANCID BEEF
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS (*HPUS) - equal amounts of: Calendula Officinalis 6X, Symphytum Officinale 6X, Arnica Montana 12X, Bellis Perennis 12X, Bryonia Alba 12X, Hypericum Perforatum 12X, Ledum Palustre 12X, Phosphorus 12X, Rhus Toxicodendron 12X, Ruta Graveolens 12X, Staphysagria 12X, Pyrogenium 30X

INDICATIONS & USAGE SECTION

USES: Temporarily relieves minor soreness, and/or aching feeling.**

OTC - PURPOSE SECTION

USES: Temporarily relieves minor soreness, and/or aching feeling.**

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS: Adults & children above 12 years: 10 drops orally 3 times daily, or as directed by a health care professional.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away.

WARNINGS SECTION

WARNINGS:

  • Consult a physician for use in children under 12 years of age.
  • IF PREGNANT OR BREAST-FEEDING, ask a health care professional before use.
  • KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away.
  • Do not use if TAMPER EVIDENT seal is broken or missing.

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: Ethyl Alcohol USP, Purified Water

OTC - QUESTIONS SECTION

QUESTIONS & COMMENTS?

Natural Creations, Inc. / Woodbine, IA 51579 / 712-647-1600

REFERENCES SECTION

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

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC:43406-0603-1

Injury

HOMEOPATHIC

1 fl oz (30mL) / 20% Alcohol

image descriptionimage description

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130877730001696GTIN-13: 0877730001696
EAN-13: 0877730001696
GTIN-12: 877730001696
UPC-A: 877730001696
GTIN storage (14 digits): 00877730001696
Injury.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43406-0603-1Injury30 mL in 1 BOTTLE, DROPPERLIQUID302

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43406-060343406-0603-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 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
InjuryCALENDULA OFFICINALIS, SYMPHYTUM OFFICINALE, ARNICA MONTANA, BELLIS PERENNIS, BRYONIA ALBA, HYPERICUM PERFORATUM, LEDUM PALUSTRE, PHOSPHORUS, RHUS TOXICODENDRON, RUTA GRAVEOLENS, STAPHYSAGRIA, PYROGENIUMNatural Creations, Incb4b850fb-6fdd-47b7-8a6e-2e596ec6256c2025-12-16WarningsExact identifier
ndc (package): 43406-0603-1
ndc (product): 43406-0603
ndc11 (package): 43406060301
spl id: b4ca5042-7e08-462f-83c5-ad38b4f7a5b2
spl set id: b4b850fb-6fdd-47b7-8a6e-2e596ec6256c

Reported adverse events (FAERS/openFDA)#

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