NDC 59667-0026 Fever And Flu

Product Information

Product Packages

NDC 59667-0026-2

Package Description: 30 [hp_C] in 1 BOTTLE, SPRAY

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Product Details

Fever And Flu is product labeled by Home Sweet Homeopathics. The product's dosage form is and is administered via form.


What are Fever And Flu Active Ingredients?

The following is the list of active ingredients in this product. An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

  • ASAFETIDA (UNII: W9FZA51AS1)
  • ASAFETIDA (UNII: W9FZA51AS1) (Active Moiety)
  • CANNABIS SATIVA SUBSP. INDICA TOP (UNII: FTS5RM302N)
  • CANNABIS SATIVA SUBSP. INDICA TOP (UNII: FTS5RM302N) (Active Moiety)
  • CANNABIS SATIVA SUBSP. SATIVA FLOWERING TOP (UNII: 8X454SZ22D)
  • CANNABIS SATIVA SUBSP. SATIVA FLOWERING TOP (UNII: 8X454SZ22D) (Active Moiety)
  • ARABICA COFFEE BEAN (UNII: 3SW678MX72)
  • ARABICA COFFEE BEAN (UNII: 3SW678MX72) (Active Moiety)
  • HELLEBORUS FOETIDUS ROOT (UNII: 332Y7EES96)
  • HELLEBORUS FOETIDUS ROOT (UNII: 332Y7EES96) (Active Moiety)
  • IPECAC (UNII: 62I3C8233L)
  • IPECAC (UNII: 62I3C8233L) (Active Moiety)
  • IRIS VERSICOLOR ROOT (UNII: X43D4L3DQC)
  • IRIS VERSICOLOR ROOT (UNII: X43D4L3DQC) (Active Moiety)
  • CANIS LUPUS FAMILIARIS MILK (UNII: G39P120JQT)
  • CANIS LUPUS FAMILIARIS MILK (UNII: G39P120JQT) (Active Moiety)
  • MENTHA PIPERITA (UNII: 79M2M2UDA9)
  • MENTHA PIPERITA (UNII: 79M2M2UDA9) (Active Moiety)
  • SODIUM SULFATE (UNII: 0YPR65R21J)
  • SODIUM SULFATE ANHYDROUS (UNII: 36KCS0R750) (Active Moiety)
  • CERVUS ELAPHUS HORN OIL (UNII: 7A7G0PQI12)
  • CERVUS ELAPHUS HORN OIL (UNII: 7A7G0PQI12) (Active Moiety)
  • OPIUM (UNII: 37M3MZ001L)
  • OPIUM (UNII: 37M3MZ001L) (Active Moiety)
  • PHOSPHORIC ACID (UNII: E4GA8884NN)
  • PHOSPHORIC ACID (UNII: E4GA8884NN) (Active Moiety)
  • SCABIES LESION LYSATE (HUMAN) (UNII: 5UAU16Z1U4)
  • SCABIES LESION LYSATE (HUMAN) (UNII: 5UAU16Z1U4) (Active Moiety)
  • SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508)
  • SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508) (Active Moiety)
  • SENECIO VULGARIS (UNII: W6MU8IYV12)
  • SENECIO VULGARIS (UNII: W6MU8IYV12) (Active Moiety)
  • CALCIUM SULFATE (UNII: WAT0DDB505)
  • CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
  • SOLANUM DULCAMARA TOP (UNII: KPS1B1162N)
  • SOLANUM DULCAMARA TOP (UNII: KPS1B1162N) (Active Moiety)
  • EUPHRASIA STRICTA (UNII: C9642I91WL)
  • EUPHRASIA STRICTA (UNII: C9642I91WL) (Active Moiety)
  • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
  • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
  • GRAPHITE (UNII: 4QQN74LH4O)
  • GRAPHITE (UNII: 4QQN74LH4O) (Active Moiety)
  • CALCIUM SULFIDE (UNII: 1MBW07J51Q)
  • CALCIUM SULFIDE (UNII: 1MBW07J51Q) (Active Moiety)
  • HYDRASTIS CANADENSIS WHOLE (UNII: R763EBH88T)
  • HYDRASTIS CANADENSIS WHOLE (UNII: R763EBH88T) (Active Moiety)
  • POTASSIUM DICHROMATE (UNII: T4423S18FM)
  • DICHROMATE ION (UNII: 9LKY4BFN2V) (Active Moiety)
  • POTASSIUM IODIDE (UNII: 1C4QK22F9J)
  • IODIDE ION (UNII: 09G4I6V86Q) (Active Moiety)
  • LYCOPODIUM CLAVATUM WHOLE (UNII: 005ICF6L27)
  • LYCOPODIUM CLAVATUM WHOLE (UNII: 005ICF6L27) (Active Moiety)
  • GONORRHEAL URETHRAL SECRETION HUMAN (UNII: 9BZG9E3I8F)
  • GONORRHEAL URETHRAL SECRETION HUMAN (UNII: 9BZG9E3I8F) (Active Moiety)
  • MERCURIUS SOLUBILIS (UNII: 324Y4038G2)
  • MERCURIUS SOLUBILIS (UNII: 324Y4038G2) (Active Moiety)
  • STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
  • STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
  • PULSATILLA VULGARIS (UNII: I76KB35JEV)
  • PULSATILLA VULGARIS (UNII: I76KB35JEV) (Active Moiety)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • COLLOIDAL SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
  • THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
  • THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
  • ACONITUM NAPELLUS (UNII: U0NQ8555JD)
  • ACONITUM NAPELLUS (UNII: U0NQ8555JD) (Active Moiety)
  • ARSENIC ACID (UNII: N7CIZ75ZPN)
  • ARSENIC ACID (UNII: N7CIZ75ZPN) (Active Moiety)
  • BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU)
  • BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU) (Active Moiety)
  • ATROPA BELLADONNA (UNII: WQZ3G9PF0H)
  • ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (Active Moiety)
  • BRYONIA ALBA ROOT (UNII: T7J046YI2B)
  • BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
  • CHELIDONIUM MAJUS (UNII: 7E889U5RNN)
  • CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (Active Moiety)
  • EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E)
  • EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E) (Active Moiety)
  • FERRUM PHOSPHORICUM (UNII: 91GQH8I5F7)
  • FERRUM PHOSPHORICUM (UNII: 91GQH8I5F7) (Active Moiety)
  • INFLUENZA A VIRUS (UNII: R9HH0NDE2E)
  • INFLUENZA A VIRUS (UNII: R9HH0NDE2E) (Active Moiety)
  • INFLUENZA B VIRUS (UNII: 1314JZ2X6W)
  • INFLUENZA B VIRUS (UNII: 1314JZ2X6W) (Active Moiety)
  • NAJA NAJA VENOM (UNII: ZZ4AG7L7VM)
  • NAJA NAJA VENOM (UNII: ZZ4AG7L7VM) (Active Moiety)
  • CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE (UNII: RN2HC612GY)
  • CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE (UNII: RN2HC612GY) (Active Moiety)
  • PHOSPHORUS (UNII: 27YLU75U4W)
  • PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)


Inactive Ingredient(s)

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)
  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)
  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)


* Please review the disclaimer below.

Fever And Flu Labeling and Warnings

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Table of Contents



Package Label.Principal Display Panel




Otc - Purpose



For symptoms associated with


For Symptoms Associated With:



To be used according to label indications.


Directions:



Spritz 1 time under the tongue 3 x per day until improvement is seen, dose once each time symptoms return.


Otc - Keep Out Of Reach Of Children



Keep out of reach of children.


Warnings



If no improvement is seen after 7 days or new symptoms develop, discontinue use.


Active Ingredients:



listed for each remedy.


Inactive Ingredients:



In reverse osmosis water with less than 1% alcohol.


* Please review the disclaimer below.