NATURASIL SCABIES- sulfur liquid

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)

Available from:

Nature's Innovation, Inc.

Administration route:

TOPICAL

Prescription type:

OTC DRUG

Therapeutic indications:

Purpose Scabies Symptom Relief Us es: Symptomatic treatment of scabies.

Authorization status:

unapproved homeopathic

Summary of Product characteristics

NATURASIL SCABIES- SULFUR 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._
----------
SCABIES TOPICAL LIQUID 50 ML LABEL
_DRUG FACTS_
_ACTIVE INGREDIENTS:_
Sulfur 6X HPUS
_The letters HPUS indicate the component(s) in this product is (are)
officially monographed in the_
_Homeopathic Pharmacopeia of the United States._
_PURPOSE_
Scabies Symptom Relief
_USES:_Symptomatic treatment of scabies.
_WARNINGS:_ FOR EXTERNAL USE ONLY.
Ask a doctor before use if pregnant or nursing.
Avoid using near eyes, mouth or mucous membranes.
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:_ Add 10-20 drops to bath water. Soak for 20 minutes, air
dry. May be used for spot treatment.
To speed relief, we recommend Naturasil Sulfur Lavender Soap. Some
individuals may be sensitive to
essential oils. Skin test for tolerability. If irritation or reaction
occurs, discontinue use.
_INACTIVE INGREDIENTS:_ Cymbopogon Citratus Leaf Oil, Melaleuca
Alternifolia Leaf Oil.
_QUESTIONS? COMMENTS?_ www.naturasil.com 866.371.2499 Mfd. by:
Nature's Innovation, INc. 2723 Brickton North Dr., Buford, GA 30518
Not tested on animals.
100% NATURAL PLANT EXTRACTS
NATURASIL
50ml (1.70 fl.oz.)
TOPICAL LIQUID
HOMEOPATHIC MEDICINE
SCABIES
NATURASIL SCABIES
sulfur liquid
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:10 8 9 3-342
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
SULFUR (UNII: 70 FD1KFU70 ) (SULFUR - UNII:70 FD1KFU70 )
SULFUR
6 [hp_X]
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
WEST INDIAN LEMO NGRASS O IL (UNII: 5BIA40 E9 ED)
TEA TREE O IL (UNII: VIF56 5UC2G)
PACKAG ING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START DATE
MARKETING END DATE
1
NDC:10 8 9 3-