NDC 68428-006 Dry Eyes

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  2. Washington Homeopathic Products
  3. NDC: 68428-006 Dry Eyes

NDC Product Code 68428-006

NDC CODE: 68428-006

Proprietary Name: Dry Eyes 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: 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.

Product Characteristics

Color(s):
WHITE (C48325 - WHITE)

NDC Code Structure

  • 68428 - Washington Homeopathic Products

NDC 68428-006-14

Package Description: 300 PELLET in 1 BOTTLE, PLASTIC

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

NDC Product Information

Dry Eyes with NDC 68428-006 is a product labeled by Washington Homeopathic Products. The generic name of Dry Eyes is . The product's dosage form is and is administered via form.

Labeler Name: Washington Homeopathic Products

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.
  • SUCROSE (UNII: C151H8M554)
  • LACTOSE (UNII: J2B2A4N98G)

Product Labeler Information

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

Labeler Name: Washington Homeopathic Products
Labeler Code: 68428
Start Marketing Date: 08-20-2010 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 - INACTIVATED, the listing data was inactivated by the FDA. 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".

* Please review the disclaimer below.

Dry Eyes Product Label Images

Dry Eyes 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

PULSATILLA    6CSILICEA    6CSULPHUR       6C

Uses

To relieve the symptoms of eyes feel  itchy, scratchy and dry. Can be seasonal or result from allergic reaction.

Keep Out Of Reach Of Children

Keep this and all medicines out of reach of children.

Indications

Indications: PULSATILLA    weepingSILICEA    Formation of pusSULPHUR       Skin problems

Stop Use And Ask Doctor

If symptoms persist/worsen or if pregnant/nursing, stop use and consult your practitioner.

Directions

Adults 2 pellets every 3 hours for 2 days. Then 2 pellets morning and night for 2 weeks. Children: 1 pellet. Repeat as necessary.

Inactive Ingredients

Sucrose/Lactose

* Please review the disclaimer below.