NDC 65003-008 Starcap Medical Private Limited

NDC Product Code 65003-008

NDC 65003-008-01

Package Description: 1 g in 1 PACKET

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

NDC Product Information

Starcap Medical Private Limited with NDC 65003-008 is a product labeled by Starcap Medical Private Limited. The generic name of Starcap Medical Private Limited is . The product's dosage form is and is administered via form.

Labeler Name: Starcap Medical Private Limited

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.

  • 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: Starcap Medical Private Limited
Labeler Code: 65003
Start Marketing Date: 06-06-2014 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: 12-31-2018 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.

Starcap Medical Private Limited Product Label Images

Starcap Medical Private Limited 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 Ingredients

Isopropyl alcohol 70% v/v

Purpose

Antiseptic

Use:

For preparation of the skin prior to injection; to decrease germs in minor cuts and scrapes.

Warnings:

  • For external use only. Flammable; keep away from fire and flame.

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center immediately.

Caution:

Do not apply to irritated skin.

Do Not Use

In the eyes, or on mucous membranes. In case of deep or puncture wounds, consult a doctor.

Directions:

Wipe injection site vigorously.

Other Information:

Store at room temperature

Inactive Ingredients:

Water

* Please review the disclaimer below.