Naturasil

Manufacturer
Nature's Innovation, Inc.
Effective date
2012-02-02
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-02 01:49:42

Label at a glance#

ProductNaturasil Eczema
Active ingredientSODIUM CHLORIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

DrugFacts

Active Ingredients:

Natrum Muriaticum 6X HPUS

DESCRIPTION SECTION

The letters HPUS indicate the component(s) in this product is (are) officially monographed in the Homeopathic Pharmacopeia of the United States.

OTC - PURPOSE SECTION

Purpose

Eczema Symptom Relief

INDICATIONS & USAGE SECTION

Uses: Symptomatic treatment of eczema. 

WARNINGS SECTION

Warnings:  For external use only.

OTC - ASK DOCTOR SECTION

Ask a doctor before use if pregnant or nursing.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OTC - DO NOT USE SECTION

Do not use if tamper evident seal is broken.

OTHER SAFETY INFORMATION

In case on ingestion call Poison Control Center hotline immediately at 1-800-222-1222.

DOSAGE & ADMINISTRATION SECTION

Directions:  Apply a few drops of product to the affected area 2-3 times per day, until the eczema symptoms have cleared. It can take from several days to weeks to heal the eczema. Some individuals may be sensitive to essential oils. Skin test for tolerability. If irritation or reaction occurs, discontinue use.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Borage Seed Oil, Carrot Seed Oil, Chamomile Flower Oil, Helicrysum Flower Oil, Jojoba Seed Oil, Lavender Oil, Melaleuca Alternifolia Leaf Oil, Rose Hip Seed Oil. 

OTC - QUESTIONS SECTION

Questions? Comments?

www.naturasil.com 1-866-371-2499

Mfd. by: Nature's Innovation, Inc.

2723 Brickton North Dr., Buford, GA  30518

Not tested on animals.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC# 10893-150-
100%
Natural Plant
Extracts

Naturasil

10ml (.34 fl. oz.)
Topical Liquid
Homeopathic Medicine
Eczema

Naturasil Eczema 10 ml bottle front label
Naturasil Eczema 10 ml bottle front label
Naturasil Eczema 10 ml bottle peel out label
Naturasil Eczema 10 ml bottle peel out label
Naturasil Eczema 15 ml bottle label
Naturasil Eczema 15 ml bottle label






FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10893-150-102020-02-04C16284748780-19d75b9d0-b383-f424-e053-dadaa90a57ceEczema Label
10893-150-152020-02-04C16284748780-19d75b9d0-b383-f424-e053-dadaa90a57ceEczema Label
10893-150-102020-01-31C16284748780-19d75b9d0-b383-f424-e053-dadaa90a57ceEczema Label
10893-150-152020-01-31C16284748780-19d75b9d0-b383-f424-e053-dadaa90a57ceEczema Label

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
SODIUM CHLORIDEACTIVE INGREDIENT451W47IQ8X3
SODIUMACTIVE MOIETY9NEZ333N273
BORAGE OILINACTIVE INGREDIENTF8XAG1755S3
CARROT SEED OILINACTIVE INGREDIENT595AO13F113
CHAMOMILE FLOWER OILINACTIVE INGREDIENT60F80Z61A93
HELICHRYSUM ITALICUM FLOWER OILINACTIVE INGREDIENTO97ZV7726K3
JOJOBA OILINACTIVE INGREDIENT724GKU717M3
LAVENDER OILINACTIVE INGREDIENTZBP1YXW0H83
ROSA RUBIGINOSA SEED OILINACTIVE INGREDIENT8M1P49MWAP3
TEA TREE OILINACTIVE INGREDIENTVIF565UC2G3

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10893-15010893-150-10, 10893-150-15

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
LAVENDER OILLAVENDER OILZBP1YXW0H8INHALANT / NASALNAExact identifier — unii candidate
2 equally ranked IID candidates
LAVENDER OILLAVENDER OILZBP1YXW0H8GEL / TOPICAL0.1 %w/wExact identifier — unii candidate
2 equally ranked IID candidates

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
fab0ab29-1f86-495f-829e-385594f5352e5c17f913-bb5c-4b91-bae8-2f7bbb946b722012-02-02WarningsExact identifier
spl id: fab0ab29-1f86-495f-829e-385594f5352e
spl set id: 5c17f913-bb5c-4b91-bae8-2f7bbb946b72

Reported adverse events (FAERS/openFDA)#

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