NDC 55714-1114 Sick Stopper

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
55714-1114
Proprietary Name:
Sick Stopper
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Newton Laboratories, Inc.
Labeler Code:
55714
Start Marketing Date: [9]
03-01-2011
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 55714-1114-0

Package Description: 7.08 g in 1 BOTTLE, GLASS

NDC Code 55714-1114-1

Package Description: 28.35 g in 1 BOTTLE, GLASS

NDC Code 55714-1114-2

Package Description: 56.7 g in 1 BOTTLE, GLASS

Product Details

What is NDC 55714-1114?

The NDC code 55714-1114 is assigned by the FDA to the product Sick Stopper which is product labeled by Newton Laboratories, Inc.. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 55714-1114-0 7.08 g in 1 bottle, glass , 55714-1114-1 28.35 g in 1 bottle, glass , 55714-1114-2 56.7 g in 1 bottle, glass . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Sick Stopper?

Sick Stopper    Formulated for symptoms associated with colds and infections.  Begin at the onset of symptoms.

Which are Sick Stopper UNII Codes?

The UNII codes for the active ingredients in this product are:

  • BACILLUS ANTHRACIS IMMUNOSERUM RABBIT (UNII: 41LZ22DD4N)
  • BACILLUS ANTHRACIS IMMUNOSERUM RABBIT (UNII: 41LZ22DD4N) (Active Moiety)
  • INFLUENZA A VIRUS (UNII: R9HH0NDE2E)
  • INFLUENZA A VIRUS (UNII: R9HH0NDE2E) (Active Moiety)
  • RANCID BEEF (UNII: 29SUH5R3HU)
  • RANCID BEEF (UNII: 29SUH5R3HU) (Active Moiety)
  • BUFO BUFO CUTANEOUS GLAND (UNII: Q59QU6N72Q)
  • BUFO BUFO CUTANEOUS GLAND (UNII: Q59QU6N72Q) (Active Moiety)
  • ACONITUM NAPELLUS (UNII: U0NQ8555JD)
  • ACONITUM NAPELLUS (UNII: U0NQ8555JD) (Active Moiety)
  • AMANITA MUSCARIA VAR. MUSCARIA FRUITING BODY (UNII: DIF093I037)
  • AMANITA MUSCARIA VAR. MUSCARIA FRUITING BODY (UNII: DIF093I037) (Active Moiety)
  • AMERICAN GINSENG (UNII: 8W75VCV53Q)
  • AMERICAN GINSENG (UNII: 8W75VCV53Q) (Active Moiety)
  • BAPTISIA TINCTORIA (UNII: 5K1UO2888Y)
  • BAPTISIA TINCTORIA (UNII: 5K1UO2888Y) (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)
  • CALCIUM SULFIDE (UNII: 1MBW07J51Q)
  • CALCIUM SULFIDE (UNII: 1MBW07J51Q) (Active Moiety)
  • LACHESIS MUTA VENOM (UNII: VSW71SS07I)
  • LACHESIS MUTA VENOM (UNII: VSW71SS07I) (Active Moiety)
  • LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
  • LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
  • STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
  • STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
  • TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
  • TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
  • SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508)
  • SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508) (Active Moiety)
  • SULFUR (UNII: 70FD1KFU70)
  • SULFUR (UNII: 70FD1KFU70) (Active Moiety)
  • THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
  • THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
  • ECHINACEA, UNSPECIFIED (UNII: 4N9P6CC1DX)
  • ECHINACEA, UNSPECIFIED (UNII: 4N9P6CC1DX) (Active Moiety)
  • INFLUENZA B VIRUS (UNII: 1314JZ2X6W)
  • INFLUENZA B VIRUS (UNII: 1314JZ2X6W) (Active Moiety)

Which are Sick Stopper Inactive Ingredients UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".