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  4. NDC Product Code: 42961-035 Zee 3-in-one First Aid Antibiotic

NDC 42961-035 Zee 3-in-one First Aid Antibiotic

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 42961-035?
  5. Zee 3-in-one First Aid Antibiotic Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
42961-035
Proprietary Name:
Zee 3-in-one First Aid Antibiotic
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cintas Corporation
Labeler Code:
42961
Product Label ID:
5e4cd139-2ea6-45ec-afb5-97b42c639755
Start Marketing Date: [9]
07-12-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Code Structure Chart

Product Details

What is NDC 42961-035?

The NDC code 42961-035 is assigned by the FDA to the product Zee 3-in-one First Aid Antibiotic which is product labeled by Cintas Corporation. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 42961-035-02 10 packet in 1 box / 900 mg in 1 packet (42961-035-01), 42961-035-03 6 packet in 1 box / 900 mg in 1 packet (42961-035-01). 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 Zee 3-in-one First Aid Antibiotic?

Clean the affected areaapply a small amount (equal to surface area of tip of finger) on area 1 to 3 times dailymay be covered with a sterile bandage

Which are Zee 3-in-one First Aid Antibiotic UNII Codes?

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

Which are Zee 3-in-one First Aid Antibiotic 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".