NDC 80353-195 Herbciti Immunies

Homeopathic Immunomodulator

NDC Product Code 80353-195

NDC CODE: 80353-195

Proprietary Name: Herbciti Immunies What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Homeopathic Immunomodulator What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

Product Characteristics

Color(s):
GREEN (C48329)
Shape: CAPSULE (C48336)
Size(s):
22 MM
Score: 1

NDC Code Structure

  • 80353 - Herbciti Llc

NDC 80353-195-01

Package Description: 1 CAPSULE in 1 BOTTLE, GLASS > 54 CAPSULE in 1 CAPSULE (80353-195-02)

NDC Product Information

Herbciti Immunies with NDC 80353-195 is a a human over the counter drug product labeled by Herbciti Llc. The generic name of Herbciti Immunies is homeopathic immunomodulator. The product's dosage form is capsule and is administered via oral form.

Dosage Form: Capsule - A solid oral dosage form consisting of a shell and a filling. The shell is composed of a single sealed enclosure, or two halves that fit together and which are sometimes sealed with a band. Capsule shells may be made from gelatin, starch, or cellulose, or other suitable materials, may be soft or hard, and are filled with solid or liquid ingredients that can be poured or squeezed.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Herbciti Immunies Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.


Inactive Ingredient(s)

About the 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.

  • SAURURUS CHINENSIS WHOLE (UNII: 6DRV3D37XS)
  • PLANTAGO ASIATICA (UNII: 5F5728J5E8)
  • LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)
  • GREEN TEA LEAF (UNII: W2ZU1RY8B0)
  • BEAN (UNII: 8WB9PV3YW5)
  • PORTULACA OLERACEA LEAF (UNII: 9JW9D9JGHZ)
  • ANGELICA SINENSIS ROOT (UNII: B66F4574UG)
  • GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
  • TARAXACUM OFFICINALE (UNII: 39981FM375)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

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

Labeler Name: Herbciti Llc
Labeler Code: 80353
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 10-20-2021 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2022 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.

Exclude Flag: N - NO 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".

* Please review the disclaimer below.

Herbciti Immunies Product Label Images

Herbciti Immunies Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredient

Panax Ginseng 40%

Purpose

Promotes anti-oxidant, anti-inflammatory, and immunomodulatory support

Keep Out Of Reach Of Children

Keep out of reach of children

Directions

Take three (3) capsules three times a day.

Use

  • To balance immune responseTo support immune healthTo promote anti-inflammatory, and anti-oxidant support

Inactive Ingredients

Asian Lizard’s Tail (Saururus chinensis), Asiatin Plantain (Plantago asiatica), Purslane (Portulaca oleracea) Leaf, Japanese Honeysuckle (Lonicera japonica) Flower, Green Tea Leaf, Bean, Dandelion (Taraxacum officinale), Dong Quai (Angelica sinensis)Root, Licorice (Glycyrrhiza glabra), Lactobacillus acidophilus, Streptococcus Thermophilus, Bifidobacterium longum

Warning

Individuals with known medical conditions should consult a doctor prior to using this.

Other Information

  • Do not use if seal is broken.Do not eat freshness packet enclosed.Keep product out of direct sunlight, high temperature, and humidity.Store in a cool, dry place.

Package Label Display

​Herbciti ImmuniesHerbal ImmunomodulatorAnti-Inflammatory SupportAnti-Oxidant SupportHomeopathic 54 Capsules

* Please review the disclaimer below.