Label: OSTEODORON PM BONE SUPPORT- oyster shell calcium carbonate, crude white oak bark calcium fluoride silicon dioxide powder
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Contains inactivated NDC Code(s)
NDC Code(s): 48951-7097-4 - 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 March 12, 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
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INGREDIENTS AND APPEARANCE
OSTEODORON PM BONE SUPPORT
oyster shell calcium carbonate, crude white oak bark calcium fluoride silicon dioxide powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-7097 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I) OYSTER SHELL CALCIUM CARBONATE, CRUDE 1 [hp_X] WHITE OAK BARK (UNII: 93LP7Y8EGT) (WHITE OAK BARK - UNII:93LP7Y8EGT) WHITE OAK BARK 4 [hp_X] CALCIUM FLUORIDE (UNII: O3B55K4YKI) (CALCIUM FLUORIDE - UNII:O3B55K4YKI) CALCIUM FLUORIDE 6 [hp_X] SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE 6 [hp_X] Inactive Ingredients Ingredient Name Strength LACTOSE (UNII: J2B2A4N98G) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:48951-7097-4 1 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