NDC 73390-101 Tilcare

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:
73390-101
Proprietary Name:
Tilcare
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Tilco Trading Pte. Ltd.
Labeler Code:
73390
Start Marketing Date: [9]
10-23-2019
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 73390-101-15

Package Description: 1 BOTTLE in 1 BOX / 15 mL in 1 BOTTLE (73390-101-14)

NDC Code 73390-101-20

Package Description: 2 BOTTLE in 1 BOX / 15 mL in 1 BOTTLE (73390-101-14)

Product Details

What is NDC 73390-101?

The NDC code 73390-101 is assigned by the FDA to the product Tilcare which is product labeled by Tilco Trading Pte. Ltd.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 73390-101-15 1 bottle in 1 box / 15 ml in 1 bottle (73390-101-14), 73390-101-20 2 bottle in 1 box / 15 ml in 1 bottle (73390-101-14). 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 Tilcare?

FOR USE IN THE EAR ONLY.• adults and children over 12 years of age: tilt head sideways and place 5 to 10 drops into ear. Tip of applicator should not enter ear canal. Keep drops in ear for several minutes by keeping head tilted or placing cotton in the ear. Use twice daily for up to 4 days if needed, or as directed by a doctor. Any wax remaining after treatment may be removed by gently flushing the ear with warm water, using a soft rubber bulb ear syringe.• children under 12 years of age: consult a doctor.

Which are Tilcare UNII Codes?

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

Which are Tilcare 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:

What is the NDC to RxNorm Crosswalk for Tilcare?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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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".