Label: CARTILAGO BETULA ADULT SIZE SPECIAL ORDER suppository
- NDC Code(s): 48951-3200-1
- Packager: Uriel Pharmacy Inc.
- Category: HUMAN OTC 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 April 24, 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. Contains traces of 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 seals on box are broken or missing.
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INGREDIENTS AND APPEARANCE
CARTILAGO BETULA ADULT SIZE SPECIAL ORDER
cartilago betula adult size special order suppositoryProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-3200 Route of Administration RECTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BETULA PUBESCENS LEAF (UNII: 84SOH0O3OO) (BETULA PUBESCENS LEAF - UNII:84SOH0O3OO) BETULA PUBESCENS LEAF 5 [hp_X] in 1 g BOS TAURUS CARTILAGE (UNII: UE77B10IIY) (BOS TAURUS CARTILAGE - UNII:UE77B10IIY) BOS TAURUS CARTILAGE 6 [hp_X] in 1 g TIN (UNII: 387GMG9FH5) (TIN - UNII:387GMG9FH5) TIN 8 [hp_X] in 1 g GOLD (UNII: 79Y1949PYO) (GOLD - UNII:79Y1949PYO) GOLD 10 [hp_X] in 1 g ONION (UNII: 492225Q21H) (ONION - UNII:492225Q21H) ONION 15 [hp_X] in 1 g FORMICA RUFA (UNII: 55H0W83JO5) (FORMICA RUFA - UNII:55H0W83JO5) FORMICA RUFA 15 [hp_X] in 1 g Inactive Ingredients Ingredient Name Strength COCOA BUTTER (UNII: 512OYT1CRR) SORBITAN MONOLAURATE (UNII: 6W9PS8B71J) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) LACTOSE (UNII: J2B2A4N98G) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:48951-3200-1 10 in 1 BOX 09/01/2009 1 2 g in 1 BLISTER PACK; 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(48951-3200)
