Label: ALEROFF- histamine liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 81701-111-01 - Packager: OKSALUD COLOMBIA S A S
- 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 24, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- WARNINGS
- INACTIVE INGREDIENT
- DOSAGE & ADMINISTRATION
- TROUBLESHOOTING
- INFORMATION FOR PATIENTS
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- KEEP OUT OF REACH OF CHILDREN
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ALEROFF
histamine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81701-111 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HISTAMINE (UNII: 820484N8I3) (HISTAMINE - UNII:820484N8I3) HISTAMINE 7 g in 7 mL Inactive Ingredients Ingredient Name Strength TUSSILAGO FARFARA FLOWER (UNII: UEE27X2Q2M) 7 mL in 7 mL ALCOHOL (UNII: 3K9958V90M) 7 mL in 7 mL CALADIUM BICOLOR WHOLE (UNII: 66BMR064Z9) 7 mL in 7 mL RANUNCULUS BULBOSUS ROOT (UNII: XV11P9Y1A1) 7 mL in 7 mL URTICA DIOICA (UNII: 710FLW4U46) 7 mL in 7 mL SOLANUM LYCOPERSICUM WHOLE (UNII: 0243Q4990L) 7 mL in 7 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81701-111-01 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 03/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 03/01/2021 Labeler - OKSALUD COLOMBIA S A S (885622207) Registrant - OKSALUD COLOMBIA S A S (885622207) Establishment Name Address ID/FEI Business Operations OKSALUD COLOMBIA S A S 885622207 manufacture(81701-111) , label(81701-111)
