NDC 70000-0017 Leader Lubricant Eye Drops 30ct

Polyethylene Glycol 400, Propylene Glycol

NDC Product Code 70000-0017

NDC Code: 70000-0017

Proprietary Name: Leader Lubricant Eye Drops 30ct 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: Polyethylene Glycol 400, Propylene Glycol 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.

NDC Code Structure

  • 70000 - Cardinal Health
    • 70000-0017 - Leader Lubricant Eye Drops 30ct

NDC 70000-0017-1

Package Description: 30 VIAL, SINGLE-USE in 1 BOX > .4 mL in 1 VIAL, SINGLE-USE

NDC Product Information

Leader Lubricant Eye Drops 30ct with NDC 70000-0017 is a a human over the counter drug product labeled by Cardinal Health. The generic name of Leader Lubricant Eye Drops 30ct is polyethylene glycol 400, propylene glycol. The product's dosage form is liquid and is administered via ophthalmic form.

Labeler Name: Cardinal Health

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

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.

Leader Lubricant Eye Drops 30ct 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.

  • POLYETHYLENE GLYCOL 400 .4 g/100mL
  • PROPYLENE GLYCOL .3 g/100mL

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.

  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • SODIUM HYDROXIDE (UNII: 55X04QC32I)
  • HYDROCHLORIC ACID (UNII: QTT17582CB)
  • BORIC ACID (UNII: R57ZHV85D4)
  • HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
  • POTASSIUM CHLORIDE (UNII: 660YQ98I10)
  • WATER (UNII: 059QF0KO0R)

Administration Route(s)

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

  • Ophthalmic - Administration to the external eye.

Product Labeler Information

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

Labeler Name: Cardinal Health
Labeler Code: 70000
FDA Application Number: part349 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph. 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: 07-18-2019 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: 12-31-2020 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 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.

Leader Lubricant Eye Drops 30ct 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

Polyethylene glycol 400 0.4%Propylene glycol 0.3%

Purposes

LubricantLubricant

Use

  • For the temporary relief of burning and irritation of the eye due to dryness of the eye

Warnings

For external use only

Do Not Use

  • If the solution changes color or becomes cloudyif you are sensative to any ingredient in this product

When Using This Product

  • Do not touch tip of container to any surface to avoid contaminationdo not reuseonce opened, discard

Stop Use And Ask A Doctor If

  • You feel eye painchanges in vision occurredness or irritation of the eye(s) gets worse or lasts more than 72 hours

If Pregnant Or Breast-Feeding,

Ask a health professional before use.

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

  • Instill 1 or 2 drops in the affected eye(s) as needed

Other Information

  • Store at 15°-25°C (59°-77°F)use only if single-use container is intactuse before expiration date marked on containerRETAIN THIS CARTON FOR FUTURE REFERENCE

Inactive Ingredients

Boric acid, hypromellose, potassium chloride, purified water, sodium chloride. May contain sodium hydroxide and/or hydrochloric acid to adjust pH.

* Please review the disclaimer below.

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