NDC 37808-100 Heb Lubricant Eye Drops

Carboxymethylcellulose Sodium

NDC Product Code 37808-100

NDC Code: 37808-100

Proprietary Name: Heb Lubricant Eye Drops Additional informationCallout TooltipWhat 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: Carboxymethylcellulose Sodium Additional informationCallout TooltipWhat 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.


Code Structure
  • 37808 - Heb
    • 37808-100 - Heb Lubricant Eye Drops

NDC 37808-100-01

Package Description: 30 VIAL, DISPENSING in 1 CARTON > .4 mL in 1 VIAL, DISPENSING

NDC Product Information

Heb Lubricant Eye Drops with NDC 37808-100 is a a human over the counter drug product labeled by Heb. The generic name of Heb Lubricant Eye Drops is carboxymethylcellulose sodium. The product's dosage form is solution/ drops and is administered via ophthalmic form.

Labeler Name: Heb

Dosage Form: Solution/ Drops - A solution which is usually administered in a drop-wise fashion.

Product Type: Human Otc Drug Additional informationCallout TooltipWhat 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.


Heb Lubricant Eye Drops Active Ingredient(s)

Additional informationCallout TooltipWhat is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • CARBOXYMETHYLCELLULOSE SODIUM .5 g/100mL

Inactive Ingredient(s)

Additional informationCallout TooltipAbout 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.

  • CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
  • MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
  • POTASSIUM CHLORIDE (UNII: 660YQ98I10)
  • WATER (UNII: 059QF0KO0R)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • SODIUM LACTATE (UNII: TU7HW0W0QT)
  • SODIUM HYDROXIDE (UNII: 55X04QC32I)
  • HYDROCHLORIC ACID (UNII: QTT17582CB)

Administration Route(s)

Additional informationCallout TooltipWhat 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

Additional informationCallout TooltipWhat is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Heb
Labeler Code: 37808
FDA Application Number: part349 Additional informationCallout TooltipWhat 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. Additional informationCallout TooltipWhat 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: 01-11-2019 Additional informationCallout TooltipWhat 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 Additional informationCallout TooltipWhat 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 Additional informationCallout TooltipWhat 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.

Heb Lubricant Eye Drops Product Label Images

Heb Lubricant Eye Drops 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 ingredientCarboxymethylcellulose sodium 0.5%

Otc - Purpose

PurposeCarboxymethylcellulose sodium.............Lubricant

Indications & Usage

  • Usesfor the temporary relief of burning, irritation, and discomfort due to dryness of the eye or exposure to wind or sunmay be used as a protectant against further irritation

Warnings

​WarningsFor external use only.

Otc - Do Not Use

  • ​ Do not use this product ifsolution changes color or becomes cloudy

Otc - When Using

  • When using the productdo not reuseonce opened, discardto avoid contamination, do not touch tip of container to any surfacedo not touch unit-dose tip to eye

Otc - Stop Use

  • Stop use and ask a doctor ifyou experience eye painchanges in vision occurredness or irritation of the eye continuesredness or irritation of the eye worsens or persists for more than 72 hours

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If accidentally swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) immediately.

Dosage & Administration

  • Directionsto open, twist and pull tab to remove.instill 1 or 2 drops in the affected eye(s) as needed and discard containerif used for post-operative (e.g., LASIK) dryness and discomfort, follow your eye doctor’s instructions.

Other Safety Information

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

Inactive Ingredient

Inactive ingredientscalcium chloride, magnesium chloride, potassium chloride, purified water, sodiumchloride, and sodium lactate. May contain sodium hydroxide and/or hydrochloric acidto adjust pH.

* Please review the disclaimer below.

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