Naturasil by Nature's Innovation, Inc. Naturasil Shingles Label

Naturasil by

Drug Labeling and Warnings

Naturasil by is a Homeopathic medication manufactured, distributed, or labeled by Nature's Innovation, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

NATURASIL SHINGLES- natrum muriaticum liquid 
Nature's Innovation, Inc.

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

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Naturasil Shingles Label

Active Ingredients

Drug Facts

Active Ingredients:

Natrum Muriaticum 6X

Description

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

Purpose

Purpose:

Zoster Shingle

Symptom Relief

Uses

Uses:Symptomatic treatment of shingles.

Warnings

Warnings:  For external use only.

Ask a doctor before use if pregnant or nursing.

Keep out of reach of children.

Do not use if tamper evident seal is broken.

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

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

Questions

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

NDC# 10893-540-

100%
Natural Plant
Extracts

Naturasil

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

Warts

NATURASIL  SHINGLES
natrum muriaticum liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10893-750
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698)	SODIUM CHLORIDE	6 [hp_X]  in 10 mL

Inactive Ingredients
Ingredient Name	Strength
CRYPTOCARYA AGATHOPHYLLA LEAF OIL (UNII: XM00Z00H98)
JOJOBA OIL (UNII: 724GKU717M)
LAVENDER OIL (UNII: ZBP1YXW0H8)
TEA TREE OIL (UNII: VIF565UC2G)
MELISSA OFFICINALIS LEAF OIL (UNII: PTP6R7263M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10893-750-10	10 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	01/12/2012	02/01/2020
2	NDC: 10893-750-15	15 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	01/12/2012	02/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		01/12/2012	02/01/2020

Labeler - Nature's Innovation, Inc. (602969854)

Establishment
Name	Address	ID/FEI	Business Operations
Nature's Innovation, Inc.		602969854	manufacture(10893-750)

Revised: 2/2020

Document Id: 3d4ac6dd-54cd-407b-bca5-ae8fc53e6033

34390-5

Set id: 03bc8917-6b68-4aad-8430-64cabc3e2604

Version: 4

Effective Time: 20200203