Trauma Relief

Manufacturer
Deseret Biologicals | Apotheca Company
Effective date
2017-03-17
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:17:33

Label at a glance#

ProductTrauma Relief
Active ingredientMATRICARIA RECUTITA, ECHINACEA ANGUSTIFOLIA, HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK, HYPERICUM PERFORATUM, ACHILLEA MILLEFOLIUM, BRYONIA ALBA ROOT, CALENDULA OFFICINALIS FLOWERING TOP, COMFREY ROOT, ARNICA MONTANA, ATROPA BELLADONNA WHOLE, BELLIS PERENNIS, CLEMATIS VITALBA FLOWER, HELIANTHEMUM NUMMULARIUM FLOWER, IMPATIENS GLANDULIFERA FLOWER, ORNITHOGALUM UMBELLATUM FLOWERING TOP, PRUNUS CERASIFERA FLOWER, TOXICODENDRON PUBESCENS LEAF, CALCIUM SULFIDE, ACTIVATED CHARCOAL
Label structure9 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Chamomilla 3X, Echinacea (Angustifolia) 3X, Hamamelis Virginiana 3X, Hypericum Perforatum 3X, Millefolium 3X, 6X, Bryonia (Alba) 4X, Calendula Officinalis 4X, Symphytum Officinale 4X, Arnica Montana 4X, Belladonna 6X, Bellis Perennis 6X, Clematis Vitalba, Flos 6X, Helianthemum Nummularium, Flos 6X, Impatiens Glandulifera, Flos 6X, Ornithogalum Umbellatum, Flos 6X, Prunus Cerasifera, Flos 6X, Rhus Tox 6X, Hepar Sulphuris Calcareum 8X, Carbo Vegetabilis 12X.

HOMEOPATHIC INDICATIONS:

OTC - PURPOSE SECTION

For the temporary relief of strains, sprains, and 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. If swallowed, get medical help or contact a Poison Control Center right away.

If pregnant or breast-feeding, seek advice of a health professional before use.

Do not use if seal is broken or missing.

For external use only, not for oral use.

Do not expose to extreme heat.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

SUGGESTED APPLICATION:

DOSAGE & ADMINISTRATION SECTION

Apply a small amount on the area of discomfort, gently rubbing the gel into the skin. Application should be as soon after the injury as possible. Repeat three times in ten minute intervals; thereafter apply three times daily as needed.

HOMEOPATHIC INDICATIONS:

INDICATIONS & USAGE SECTION

For the temporary relief of strains, sprains, and 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, Glycerin, L-Arginine Base, Sodium PCA, Aloe Barbadensis Leaf Juice, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Benzylalcohol-DHA, Glycine, Hyaluronic Acid, L-Aspartic Acid.

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. By: Deseret Biologicals, Inc.

469 W. Parkland Drive

Sandy, UT 84070 www.desbio.com

PACKAGE DISPLAY LABEL:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DESBIO

NDC 43742-0322-1

HOMEOPATHIC

TRAUMA

RELIEF GEL

With Aloe Vera

NET WT 4.44 OZ (126 G)

Trauma Relief GelTrauma Relief Gel

Products#

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

DailyMed product names page 1 of 1 · 32 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43742-067043742-0670-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 30 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
862184cf-4c6e-4787-a71c-c16a1dad1d2fe4b91839-61bf-45df-9513-c59d8f73d7e72017-03-17WarningsExact identifier
spl id: 862184cf-4c6e-4787-a71c-c16a1dad1d2f
spl set id: e4b91839-61bf-45df-9513-c59d8f73d7e7

Reported adverse events (FAERS/openFDA)#

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