NDC 77555-347 Waldo Hydration Drops

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:
77555-347
Proprietary Name:
Waldo Hydration Drops
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
77555
Start Marketing Date: [9]
08-24-2020
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 77555-347?

The NDC code 77555-347 is assigned by the FDA to the product Waldo Hydration Drops which is product labeled by Ainsly Limited. The product's dosage form is . The product is distributed in a single package with assigned NDC code 77555-347-11 1 bottle, dropper in 1 carton / 10 ml in 1 bottle, dropper. 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 Waldo Hydration Drops?

For adults and children age 2 and over:• remove tamper-evident seal from neck of bottle• twist cap off bottle• DON'T squeeze bottle, squeeze plastic tip to release 2 to 3 drops into eye• apply as needed• replace cap after use

Which are Waldo Hydration Drops UNII Codes?

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

  • CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371)
  • CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371) (Active Moiety)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
  • RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S)
  • RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S) (Active Moiety)
  • POLYGALA SENEGA ROOT (UNII: M7T6H7D4IF)
  • POLYGALA SENEGA ROOT (UNII: M7T6H7D4IF) (Active Moiety)

Which are Waldo Hydration Drops 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:

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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".