Label: MANDRAGORA 5% SPECIAL ORDER ointment
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Contains inactivated NDC Code(s)
NDC Code(s): 48951-7128-5 - 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 September 30, 2014
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- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
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WARNINGS
Warnings: FOR EXTERNAL USE ONLY. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions, if conditions worsen or persist, or accidental ingestion occurs. If pregnant or nursing, consult a doctor before use. Avoid contact with eyes. Do not use if safety seal is broken or missing.
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INGREDIENTS AND APPEARANCE
MANDRAGORA 5% SPECIAL ORDER
mandragora 5% special order ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-7128 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MANDRAGORA OFFICINARUM ROOT (UNII: I2XCB174VB) (MANDRAGORA OFFICINARUM ROOT - UNII:I2XCB174VB) MANDRAGORA OFFICINARUM ROOT 1 [hp_X] in 1 g Inactive Ingredients Ingredient Name Strength OLIVE OIL (UNII: 6UYK2W1W1E) LANOLIN (UNII: 7EV65EAW6H) PETROLATUM (UNII: 4T6H12BN9U) WATER (UNII: 059QF0KO0R) YELLOW WAX (UNII: 2ZA36H0S2V) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) CITRUS PARADISI SEED (UNII: 12F08874Y7) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:48951-7128-5 60 g in 1 TUBE 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(48951-7128)