Label: SUCROSE pellet
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Contains inactivated NDC Code(s)
NDC Code(s): 48951-9999-2 - 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 February 2, 2010
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Purpose
- Dosage & Administration
- OTC-Active 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
SUCROSE
sucrose pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-9999 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SUCROSE (UNII: C151H8M554) (SUCROSE - UNII:C151H8M554) SUCROSE 1 [hp_X] Product Characteristics Color white (white) Score no score Shape ROUND (round) Size 3mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:48951-9999-2 1350 in 1 BOTTLE, GLASS Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/01/2010 Labeler - Uriel Pharmacy Inc (043471163) Establishment Name Address ID/FEI Business Operations Uriel Pharmacy Inc 043471163 manufacture