NDC 27281-004 Immune Booster

NDC Product Code 27281-004

NDC 27281-004-96

Package Description: 30 mL in 1 BOTTLE, SPRAY

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

NDC Product Information

Immune Booster with NDC 27281-004 is a product labeled by Sunway Biotech Llc. The generic name of Immune Booster is . The product's dosage form is and is administered via form.

Labeler Name: Sunway Biotech Llc

Dosage Form: -

Product Type: 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.

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.

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

Product Labeler Information

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

Labeler Name: Sunway Biotech Llc
Labeler Code: 27281
Start Marketing Date: 11-13-2013 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: 12-31-2017 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: I 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Immune Booster Product Label Images

Immune Booster 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

Otc - Active Ingredient

Active Ingredients: Equal volumes of each ingredient: Apis Mellifica 200C HPUS, Baptisia Tinctoria 6X HPUS, Carduus Marianus 3X HPUS, DNA 6X HPUS, Echinacea 6X HPUS, Galium Aparine 3X HPUS, Mercurius Corrosivus 200C HPUS, Mercurius Sulphuratus Ruber 30C HPUS, Nitricum Acidum 30C HPUS, Sulphur Iodatum 200C, Thuja Occidentalis 200C.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Otc - Purpose

NDC #: 2728100496IMMUNE BOOSTEREnergy Medicine with DNA & EchinaceaHomeopathic Fast-Acting Oral Spray1.0 Fl Oz (30 ml)Alcohol 9% v/v

Indications & Usage

Indications: Helps support the body's natural defense mechanisms and temporarily relieves: tendencies toward flu & cold; joint pain; minor allergies; low endocrine function.

Dosage & Administration

Directions: Adults only: Spray twice under the tongue, three times a day. This bottle contains about a 1 month supply.


Warnings: keep out of reach of children. If pregnant or breast feeding, ask a doctor before using product. Stop use and ask a doctor if  symptoms persist more than 3 days, worsen, or if new symptoms occur.

Other Safety Information

Tamper Evident Seal: Do not use if seal around neck of bottle is broken or missing. The letters HPUS indicate that ingredients are officially included in the Homeopathic Pharmarcopoeia of the United States.

Inactive Ingredient

Inactive Ingredients: Alcohol 9% v/v, Glycerin 10% v/v, Purified Water.

* Please review the disclaimer below.