CROTALUS TERRIFICUS 30X liquid

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

CROTALUS DURISSUS TERRIFICUS VENOM (UNII: 2XF6I0446G) (CROTALUS DURISSUS TERRIFICUS VENOM - UNII:2XF6I0446G)

Available from:

Uriel Pharmacy, Inc.

Administration route:

ORAL

Prescription type:

OTC DRUG

Therapeutic indications:

Directions: FOR ORAL USE. Use: Temporary relief of headache.

Authorization status:

unapproved homeopathic

Summary of Product characteristics

CROTALUS TERRIFICUS 30X- CROTALUS TERRIFICUS 30X LIQUID
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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CROTALUS TERRIFICUS 30X
Directions: FOR ORAL USE.
Take the contents of one ampule under the tongue and hold for 30
seconds, then
swallow.
Active Ingredient: Crotalus terrificus e veneno (Rattlesnake venom)
30X
Inactive Ingredients: Water, Salt
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.
Consult a doctor
before use for serious conditions or if conditions worsen or persist.
If pregnant or
nursing, consult a doctor before use.
Questions? Call 866.642.2858
Uriel, East Troy, WI 53120
www.urielpharmacy.com Lot#
CROTALUS TERRIFICUS 30X
crotalus terrificus 30x liquid
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:48951-3249
ROUTE OF ADMINISTRATION
ORAL
Uriel Pharmacy, Inc.
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
CROTALUS DURISSUS TERRIFICUS VENOM (UNII: 2XF6I0446G) (CROTALUS
DURISSUS TERRIFICUS VENOM - UNII:2XF6I0446G)
CROTALUS DURISSUS
TERRIFICUS VENOM
30 [hp_X]
in 1 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
SODIUM CHLORIDE (UNII: 451W47IQ8X)
WATER (UNII: 059QF0KO0R)
PACKAGING
# ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:48951-
3249-1
10 in 1 BOX
09/01/2009
1
1 mL in 1 AMPULE; Type 1: Convenience Kit of Co-
Package
MARKETING INFORMATION
MARKETING
CATEGORY
APPLICATION NUMBER OR MONOGRAPH
CITATION
MARKETING START
DATE
MARKETING END
DATE
unapproved
homeopathic
09/01/2009
LABELER -
Uriel Pharmacy, Inc. (043471163)
ESTABLISHMENT
NAME
ADDRESS
ID/FEI
BUSINESS OPERATIONS
Uriel Pharmacy, Inc.
043471163
manufacture(48951-3249)
Revised: 10/2021