Label: QUERCUS BORAGO ADULT SIZE suppository
- NDC Code(s): 48951-8115-1
- 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 April 30, 2018
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- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
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WARNINGS
KEEP REFRIGERATED OR STORE IN COOL, DRY PLACE. REFRIGERATE TO RESOLIDIFY.
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. Do not use if safety seals on box are broken or missing. - QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
QUERCUS BORAGO ADULT SIZE
quercus borago adult size suppositoryProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-8115 Route of Administration RECTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AESCULUS HIPPOCASTANUM BARK (UNII: 7U76MXL14N) (AESCULUS HIPPOCASTANUM BARK - UNII:7U76MXL14N) AESCULUS HIPPOCASTANUM BARK 3 [hp_X] in 1 g BORAGE (UNII: PB618V0K2W) (BORAGE - UNII:PB618V0K2W) BORAGE 3 [hp_X] in 1 g MILK THISTLE (UNII: U946SH95EE) (MILK THISTLE - UNII:U946SH95EE) MILK THISTLE 3 [hp_X] in 1 g HAMAMELIS VIRGINIANA LEAF (UNII: T07U1161SV) (HAMAMELIS VIRGINIANA LEAF - UNII:T07U1161SV) HAMAMELIS VIRGINIANA LEAF 3 [hp_X] in 1 g QUERCUS ROBUR WHOLE (UNII: R7QMG0BT2W) (QUERCUS ROBUR WHOLE - UNII:R7QMG0BT2W) QUERCUS ROBUR WHOLE 1 [hp_X] in 1 g MERCURIALIS PERENNIS (UNII: Q35465A1MA) (MERCURIALIS PERENNIS - UNII:Q35465A1MA) MERCURIALIS PERENNIS 2 [hp_X] in 1 g ANTIMONY (UNII: 9IT35J3UV3) (ANTIMONY - UNII:9IT35J3UV3) ANTIMONY 3 [hp_X] in 1 g Inactive Ingredients Ingredient Name Strength COCOA BUTTER (UNII: 512OYT1CRR) CORN OIL (UNII: 8470G57WFM) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:48951-8115-1 10 in 1 BOX 09/01/2009 1 2 g in 1 BLISTER PACK; Type 0: Not a Combination Product 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(48951-8115)