SULPHUR - sulfur pellet

United States - English - NLM (National Library of Medicine)

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Active ingredient:
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)
Available from:
REMEDY MAKERS
Administration route:
SUBLINGUAL
Prescription type:
OTC DRUG
Therapeutic indications:
SULFUR
Authorization status:
unapproved homeopathic
Authorization number:
10191-1578-2

SULPHUR - sulfur pellet

REMEDY MAKERS

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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SULPHUR 6X (Sulfur)

ECZEMA RASH, ACNE, OR OTHER INDICATIONS

SULFUR

WARNING:Keep this and all medications out of reach of children.

INDICATIONS: To be use according to standard homeopathic indications, for self-limiting conditions

such as these indicated above or as directed by a physician.

WARNING: Use only if cap and seal are unbroken. If symptoms persist for more than 3 days or worsen,

discontinue (STOP) use and consult your physician. As with any drug. If you are pregnant or nursing

(breast-feeding) a baby, seek the advise of a health professional before using this product. Store tightly

closed in a cool area.

Directions:(adult/children) Dissolve 3 or 4 pellets in mouth or under tongue 3 times a day or as directed

by a physician. Children 2 years and older take 1/2 the adult dose.

Inactive Ingredient: Lactose and Sucrose. Free from yeast, wheat, corn and soy.

Questions or comments.(877)REM4YOU. Fax (909)594-4205 Pomona, CA. 91768. USA

www.remedymakers.com

Other information: Contain approx.137 - 141 pellets.

SULPHUR

sulfur pellet

Product Information

Product T ype

HUMAN OTC DRUG

Ite m Code (Source )

NDC:10 19 1-1578

Route of Administration

SUBLINGUAL

REMEDY MAKERS

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

SUCRO SE (UNII: C151H8 M554)

LACTO SE (UNII: J2B2A4N9 8 G)

Packag ing

#

Item Code

Package Description

Marketing Start Date

Marketing End Date

1

NDC:10 19 1-1578 -2

137 in 1 VIAL, GLASS

Marketing Information

Marke ting Cate gory

Application Numbe r or Monograph Citation

Marke ting Start Date

Marke ting End Date

unappro ved ho meo pathic

12/0 8 /19 9 8

Labeler -

REMEDY MAKERS (018543582)

Revised: 11/2011

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