Label: CRATAEGUS E FOL. ET FRUCTUS 2 SPECIAL ORDER liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 48951-3165-1 - Packager: Uriel Pharmacy Inc.
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
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.
Drug Label Information
Updated September 16, 2014
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- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- WARNINGS
- QUESTIONS
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INGREDIENTS AND APPEARANCE
CRATAEGUS E FOL. ET FRUCTUS 2 SPECIAL ORDER
crataegus e fol. et fructus 2 special order liquidProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:48951-3165 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HAWTHORN LEAF WITH FLOWER (UNII: 6OM09RPY36) (HAWTHORN LEAF WITH FLOWER - UNII:6OM09RPY36) HAWTHORN LEAF WITH FLOWER 2 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM CHLORIDE (UNII: 451W47IQ8X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:48951-3165-1 10 in 1 BOX 1 1 mL in 1 AMPULE 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(48951-3165)