FDA.reportPublic FDA data

NeoRelief Wound Care

Manufacturer
BioLyte Laboratories, LLC
Effective date
2026-01-27
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 02:36:53

Label at a glance#

ProductNeoRelief Wound Care
Active ingredientSALIX ALBA BARK, STELLARIA MEDIA, DAPHNE MEZEREUM BARK, URTICA URENS, ALTHAEA OFFICINALIS ROOT, HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK, HORSE CHESTNUT, CALENDULA OFFICINALIS FLOWERING TOP, EQUISETUM ARVENSE TOP
Label structure13 sections

Indications and uses

Helps reduce potential infection in minor cuts, scrapes and abrasions. For the temporary relief of itchiness and soreness. Promotoes wound healing. Indications are based on homeopathic materia medica, not clinical tests.

Dosage and administration

Wash hands before and after use; spread a thin layer of Wound Care on the clean affected area; Apply as needed 2-3 times daily.

Storage and handling

Store in a cool, dry place. Avoid direct sunlight. Tamper-evident for your protection. Use only if safety seal is intact.

Label contents#

Full prescribing information#

Drug Facts Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

All actives are HPUS* and 3X potency.

Aesculus Hipp., Calendula Off., Equisetum Arv., Symphytum Off.

Salix Alba, Setllaria Med.

Mezereum Off., Urtica Urens

Althaea Off., Hamamelis Vir.

*HPUS indicates the active ingredients are in the official Homeopathic Pharmacopeia of the United States.

WoundCareWoundCare

Purpose

OTC - PURPOSE SECTION

Promotes Wound Healing

Topical Analgesics

Reduces Itching

Anti-inflammatory

Uses

INDICATIONS & USAGE SECTION

Helps reduce potential infection in minor cuts, scrapes and abrasions.

For the temporary relief of itchiness and soreness.

Promotoes wound healing.

Indications are based on homeopathic materia medica, not clinical tests.

Warnings

WARNINGS SECTION

For external use only.

Do not use in the eyes, over very large areas of the body.

Warnings

OTC - ASK DOCTOR/PHARMACIST SECTION

Ask a doctor before use if you have deep or puncture wounds, animal bites, serious burns.

Warnings

OTC - STOP USE SECTION

Stop use and ask doctor if condition or symptoms worsen or last more than 1 week; symptoms clear up and occur again within a few days.

Warnings

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.

Directions

DOSAGE & ADMINISTRATION SECTION

Wash hands before and after use; spread a thin layer of Wound Care on the clean affected area; Apply as needed 2-3 times daily.

Other Information

STORAGE AND HANDLING SECTION

Store in a cool, dry place.

Avoid direct sunlight.

Tamper-evident for your protection. Use only if safety seal is intact.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Vera Leaf Powder, Colloidal Silver, Clove Oil, Emu Oil, Hyaluronic Acid, Methyl Glucose Dioleate, Ultrez-30 Polymer, Potassium Sorbate, Purified Water, Sodium Hydroxide

Questions or Comments?

OTC - QUESTIONS SECTION

800.538.1455

Monday-Friday, 8 a.m. - 5 p.m. EST or at neorelief.com.

Report any serious side effects to the number above.

Addtional Label Content

SPL UNCLASSIFIED SECTION

Packaging Recyclable

Made in the USA

Listed with the FDA

neorelief.com

Drug Facts peeled here

FTC disclosure: Product efficacy and claims are based on theories of homeopathy that are not supported by scientific evidence and most modern allopathic medical professionals.

BioLyte Labs Grand Rapids, MI 49534

NEO RELIEF WOUND CARE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 58368-006-06

NEO RELIEF

WOUND CARE

Homeopathic healing cream

Net Wt. 0.5 oz (14.17g)

neoneo

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58368-006-062024-10-16C16284748780-1ba0f9c33-2422-a910-e053-dadaa90a0b8571c4c9fd-e359-7c68-e053-2a95a90a3f68
58368-006-062021-01-29C16284748780-1ba0f9c33-2422-a910-e053-dadaa90a0b8571c4c9fd-e359-7c68-e053-2a95a90a3f68

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58368-006-06NeoRelief Wound Care14.17 g in 1 BOTTLE, PUMPCREAM14.176

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58368-00658368-006-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
NameUNIIKind
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
METHYL GLUCOSE DIOLEATEFA9KFJ4Z6PIACT
WATER059QF0KO0RIACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
SILVER3M4G523W1GIACT
ALOE VERA LEAFZY81Z83H0XIACT
CLOVE OIL578389D6D0IACT
EMU OIL344821WD61IACT
HYALURONIC ACIDS270N0TRQYIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
SODIUM HYDROXIDE55X04QC32IIACT
SALIX ALBA BARK205MXS71H7ACTIB
STELLARIA MEDIA2H03479QVRACTIB
DAPHNE MEZEREUM BARKX2N6E405GVACTIB
URTICA URENSIHN2NQ5OF9ACTIB
ALTHAEA OFFICINALIS ROOTTRW2FUF47HACTIB
HAMAMELIS VIRGINIANA ROOT BARK/STEM BARKT7S323PKJSACTIB
HORSE CHESTNUT3C18L6RJAZACTIB
CALENDULA OFFICINALIS FLOWERING TOP18E7415PXQACTIB
EQUISETUM ARVENSE TOP1DP6Y6B65ZACTIB

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
NeoRelief Wound CareHOMEOPATHIC HEALING CREAMBioLyte Laboratories, LLC71c4c9fd-e359-7c68-e053-2a95a90a3f682026-01-27WarningsExact identifier
ndc (package): 58368-006-06
ndc (product): 58368-006
ndc11 (package): 58368000606
spl id: 49613711-cad8-3b6a-e063-6394a90a7345
spl set id: 71c4c9fd-e359-7c68-e053-2a95a90a3f68

Reported adverse events (FAERS/openFDA)#

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