Label: BIRCH JUNIPER REJUVENATION- betula pendula leaf juniperus communis fruit syrup
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Contains inactivated NDC Code(s)
NDC Code(s): 48951-2071-9 - Packager: Uriel Pharmacy Inc
- Category: HUMAN OTC DRUG LABEL
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 February 1, 2010
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- Purpose
- Dosage & Administration
- OTC-Active Ingredient
- Inactive Ingredient
- Keep out of reach of children
- Do not use section
- Ask doctor section
- Pregnancy or breast feeding section
- Questions section
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
BIRCH JUNIPER REJUVENATION
betula pendula leaf juniperus communis fruit syrupProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-2071 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BETULA PENDULA LEAF (UNII: 5HW39H9KDH) (BETULA PENDULA LEAF - UNII:5HW39H9KDH) BETULA PENDULA LEAF 1 [hp_X] JUNIPERUS COMMUNIS FRUIT (UNII: O84B5194RL) (JUNIPERUS COMMUNIS FRUIT - UNII:O84B5194RL) JUNIPERUS COMMUNIS FRUIT 1 [hp_X] Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SUCROSE (UNII: C151H8M554) HONEY (UNII: Y9H1V576FH) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:48951-2071-9 5200 in 1 BOTTLE, GLASS 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