Label: MOMLOVE- not applicable spray
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Contains inactivated NDC Code(s)
NDC Code(s): 64249-0004-1 - Packager: VitaMed, LLC
- Category: HUMAN PRESCRIPTION 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 August 18, 2014
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS:
- INDICATIONS:
- WARNINGS:
- KEEP OUT OF REACH OF CHILDREN
- DIRECTIONS:
- INDICATIONS:
- INACTIVE INGREDIENTS:
- QUESTIONS:
- PACKAGE LABEL DISPLAY
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INGREDIENTS AND APPEARANCE
MOMLOVE
not applicable sprayProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:64249-0004 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (BERBERIS VULGARIS ROOT BARK - UNII:1TH8Q20J0U) BERBERIS VULGARIS ROOT BARK 6 [hp_X] in 1 mL MILK THISTLE (UNII: U946SH95EE) (MILK THISTLE - UNII:U946SH95EE) MILK THISTLE 3 [hp_X] in 1 mL CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (CHELIDONIUM MAJUS - UNII:7E889U5RNN) CHELIDONIUM MAJUS 6 [hp_C] in 1 mL PODOPHYLLUM (UNII: 2S713A4VP3) (PODOPHYLLUM - UNII:2S713A4VP3) PODOPHYLLUM 6 [hp_X] in 1 mL ANGUILLA ROSTRATA BLOOD SERUM (UNII: L7B16ESD1U) (ANGUILLA ROSTRATA BLOOD SERUM - UNII:L7B16ESD1U) ANGUILLA ROSTRATA BLOOD SERUM 30 [hp_C] in 1 mL SYMPHORICARPOS ALBUS FRUIT (UNII: 873JZU3ASZ) (SYMPHORICARPOS ALBUS FRUIT - UNII:873JZU3ASZ) SYMPHORICARPOS ALBUS FRUIT 200 [hp_C] in 1 mL GINGER (UNII: C5529G5JPQ) (GINGER - UNII:C5529G5JPQ) GINGER 6 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:64249-0004-1 30 mL in 1 BOTTLE, SPRAY Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/18/2014 Labeler - VitaMed, LLC (079364194) Registrant - Apotheca Company (844330915) Establishment Name Address ID/FEI Business Operations Apotheca Company 844330915 manufacture(64249-0004) , api manufacture(64249-0004) , label(64249-0004) , pack(64249-0004)