NDC 17312-182 Allergy Eyes Day And Night Relief Pack Day And Night Relief Pack

Allium Cepa,Ambrosia,Apis,Euphrasia,Histamine Hydrochloricum,Sabadilla,Sulphur Kit - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
17312-182
Proprietary Name:
Allergy Eyes Day And Night Relief Pack Day And Night Relief Pack
Non-Proprietary Name: [1]
Allium Cepa, Ambrosia, Apis, Euphrasia, Histamine Hydrochloricum, Sabadilla, Sulphur
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Kit - A packaged collection of related material.
Labeler Name: [5]
Trp Company
Labeler Code:
17312
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
04-11-2020
Listing Expiration Date: [11]
12-31-2024
Exclude Flag: [12]
N
Code Structure:
Code Navigator:

Product Packages

NDC Code 17312-182-20

Package Description: 1 KIT in 1 CARTON * 10 mL in 1 BOTTLE * 4 g in 1 TUBE

Product Details

What is NDC 17312-182?

The NDC code 17312-182 is assigned by the FDA to the product Allergy Eyes Day And Night Relief Pack Day And Night Relief Pack which is a human over the counter drug product labeled by Trp Company. The generic name of Allergy Eyes Day And Night Relief Pack Day And Night Relief Pack is allium cepa, ambrosia, apis, euphrasia, histamine hydrochloricum, sabadilla, sulphur. The product's dosage form is kit. The product is distributed in a single package with assigned NDC code 17312-182-20 1 kit in 1 carton * 10 ml in 1 bottle * 4 g in 1 tube. 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 Allergy Eyes Day And Night Relief Pack Day And Night Relief Pack?

Directions:• Suitable for adults and children ages 2 and over. Children under the age of 2: Consult a physician before use. • Wash your hands. • Squeeze out approx. 1/8 directly to the eye. • Apply before bedtime. • Homeopathic remedies may not be effective for everyone. Individual results may vary. Directions• Suitable for adults and children ages 2 and over. Children under the age of 2: Consult a physician before use. • Squeeze 1-3 drops in the eye. Use several times per day as needed. • Homeopathic remedies may not be effective for everyone. Individual results may vary.

Which are Allergy Eyes Day And Night Relief Pack Day And Night Relief Pack UNII Codes?

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

Which are Allergy Eyes Day And Night Relief Pack Day And Night Relief Pack 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:

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Product Footnotes

[1] 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.

[3] 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.

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

[8] 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.

[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".