Carbo Sulfur

CARBO SULFUR- carbo sulfur powder
Uriel Pharmacy 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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Carbo Sulfur

Directions: FOR ORAL USE ONLY.

Take 3-4 times daily. Ages 12 and older: 1/8 teaspoon. Ages 2-11: 1/16 teaspoon. Under age 2: Consult a doctor.

Active Ingredient: 100 gm contains: 5 gm Carbo betulae 2X; Sulfur 2X

Inactive Ingredient: Lactose

Use: Temporary relief of headache.

KEEP OUT OF REACH OF CHILDREN.

Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Contains lactose. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seal is broken or missing.

Questions? Call 866.642.2858
Uriel, East Troy, WI 53120
www.urielpharmacy.com

CarboSulfurPowder

CARBO SULFUR
carbo sulfur powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:48951-3025
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (ACTIVATED CHARCOAL - UNII:2P3VWU3H10)	ACTIVATED CHARCOAL	2 [hp_X] in 1 g
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)	SULFUR	2 [hp_X] in 1 g

Ingredient Name	Strength
Inactive Ingredients
LACTOSE (UNII: J2B2A4N98G)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:48951-3025-4	50 g in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	09/01/2009

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		09/01/2009

Labeler - Uriel Pharmacy Inc. (043471163)

Name	Address	ID/FEI	Business Operations
Establishment
Uriel Pharmacy Inc.		043471163	manufacture(48951-3025)