FDA.reportPublic FDA data

Naturasil

Manufacturer
Nature's Innovation, Inc.
Effective date
2012-02-01
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-02 01:49:44

Label at a glance#

ProductNaturasil Shingles
Active ingredientSODIUM CHLORIDE
Label structure9 sections

Indications and uses

Uses :   Symptomatic treatment of shingles.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Drug Facts

Active Ingredients:

Natrum Muriaticum 6X

Description

DESCRIPTION SECTION

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

Purpose

OTC - PURPOSE SECTION

Purpose:

Zoster Shingle

Symptom Relief

Uses

INDICATIONS & USAGE SECTION

Uses:  Symptomatic treatment of shingles.

Warnings

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 of ingestion call Poison Control Center hotline immediately at 1-800-222-1222.

DOSAGE & ADMINISTRATION SECTION

Directions:  Apply a few drops to affected area 2-3 times per day, including bottoms of feet, until outbreak has been relieved.  It is recommended to use Dermisil Super Lysine with this product to speed relief.  Some individuals may be sensitive to essential oils.  Skin test for tolerability.  If irritation occurs, discontinue use.

INACTIVE INGREDIENT SECTION

Inactive Ingredients:  Agathophyllum Aromatica Leaf Oil, Jojoba Seed Oil, Lavender Oil, Melaleuca Alternifolia Leaf Oil, Melissa Officinalis Leaf Oil.

Questions

OTC - QUESTIONS SECTION

Questions? Comments?

www.naturasil.com  1-866-371-2499

Mfd. by: Nature's Innovations, Inc.,

2723 Brickton North Dr., Buford, GA 30518

Not tested on animals.

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL



NDC# 10893-540-

100%
Natural Plant
Extracts

Naturasil

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

Warts

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






FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10893-750-102020-02-04C16284748780-19d75b9d1-247e-f424-e053-dadaa90a57ceNaturasil Shingles Label
10893-750-152020-02-04C16284748780-19d75b9d1-247e-f424-e053-dadaa90a57ceNaturasil Shingles Label
10893-750-102020-01-31C16284748780-19d75b9d1-247e-f424-e053-dadaa90a57ceNaturasil Shingles Label
10893-750-152020-01-31C16284748780-19d75b9d1-247e-f424-e053-dadaa90a57ceNaturasil Shingles Label

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
SODIUM CHLORIDEACTIVE INGREDIENT451W47IQ8X3
SODIUMACTIVE MOIETY9NEZ333N273
CRYPTOCARYA AGATHOPHYLLA LEAF OILINACTIVE INGREDIENTXM00Z00H983
JOJOBA OILINACTIVE INGREDIENT724GKU717M3
LAVENDER OILINACTIVE INGREDIENTZBP1YXW0H83
MELISSA OFFICINALIS LEAF OILINACTIVE INGREDIENTPTP6R7263M3
TEA TREE OILINACTIVE INGREDIENTVIF565UC2G3

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10893-75010893-750-10, 10893-750-15

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM CHLORIDE451W47IQ8XACTIB
CRYPTOCARYA AGATHOPHYLLA LEAF OILXM00Z00H98IACT
JOJOBA OIL724GKU717MIACT
LAVENDER OILZBP1YXW0H8IACT
TEA TREE OILVIF565UC2GIACT
MELISSA OFFICINALIS LEAF OILPTP6R7263MIACT

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
3e705b35-323e-4665-a498-ce9c5165974503bc8917-6b68-4aad-8430-64cabc3e26042012-02-01WarningsExact identifier
spl id: 3e705b35-323e-4665-a498-ce9c51659745
spl set id: 03bc8917-6b68-4aad-8430-64cabc3e2604

Reported adverse events (FAERS/openFDA)#

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