ANTIMONITE BELLADONNA powder

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

ANTIMONY TRISULFIDE (UNII: F79059A38U) (ANTIMONY TRISULFIDE - UNII:F79059A38U), ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H), MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ) (MATRICARIA RECUTITA - UNII:G0R4UBI2ZZ), BISMUTH SUBNITRATE (UNII: H19J064BA5) (BISMUTH CATION - UNII:ZS9CD1I8YE)

Available from:

Uriel Pharmacy Inc.

INN (International Name):

ANTIMONY TRISULFIDE

Composition:

ANTIMONY TRISULFIDE 3 [hp_X] in 1 g

Administration route:

ORAL

Prescription type:

OTC DRUG

Therapeutic indications:

Directions: FOR ORAL USE ONLY. Use: Temporary relief of upset stomach.

Authorization status:

unapproved homeopathic

Summary of Product characteristics

ANTIMONITE BELLADONNA- ANTIMONITE BELLADONNA 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._
----------
ANTIMONITE BELLADONNA
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 Ingredients: Antimonite (Nat. antimony trisulfide) 3X, Atropa
belladonna
(Nightshade) 4X, Chamomilla (Chamomile) 4X, Bismutum subnitricum
(Bismuth) 6X
Inactive Ingredient: Lactose
"prepared using rhythmical processes"
Use: Temporary relief of upset stomach.
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 shopuriel.com
ANTIMONITE BELLADONNA
antimonite belladonna powder
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:48951-1037
ROUTE OF ADMINISTRATION
ORAL
ACTIVE INGREDIENT/ACTIVE MOIETY
BASIS OF
Uriel Pharmacy Inc.
INGREDIENT NAME
BASIS OF
STRENGTH
STRENGTH
ANTIMONY TRISULFIDE (UNII: F79059A38U) (ANTIMONY TRISULFIDE -
UNII:F79059A38U)
ANTIMONY
TRISULFIDE
3 [hp_X]
in 1 g
ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA -
UNII:WQZ 3G9PF0H)
ATROPA
BELLADONNA
4 [hp_X]
in 1 g
MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ) (MATRICARIA RECUTITA -
UNII:G0R4UBI2Z Z )
MATRICARIA
RECUTITA
4 [hp_X]
in 1 g
BISMUTH SUBNITRATE (UNII: H19J064BA5) (BISMUTH CATION -
UNII:Z S9CD1I8YE)
BISMUTH
SUBNITRATE
6 [hp_X]
in 1 g
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
LACTOSE (UNII: J2B2A4N98G)
PACKAGING
# ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1