NDC 78902-302 Pearlessence Sanitizing Wipes

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:
78902-302
Proprietary Name:
Pearlessence Sanitizing Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Jocott Brands, Inc.
Labeler Code:
78902
Start Marketing Date: [9]
11-09-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 78902-302-51

Package Description: 160 APPLICATOR in 1 CONTAINER / 1 SOLUTION in 1 APPLICATOR (78902-302-11)

NDC Code 78902-302-52

Package Description: 50 APPLICATOR in 1 CONTAINER / 1 SOLUTION in 1 APPLICATOR (78902-302-11)

Product Details

What is NDC 78902-302?

The NDC code 78902-302 is assigned by the FDA to the product Pearlessence Sanitizing Wipes which is product labeled by Jocott Brands, Inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 78902-302-51 160 applicator in 1 container / 1 solution in 1 applicator (78902-302-11), 78902-302-52 50 applicator in 1 container / 1 solution in 1 applicator (78902-302-11). 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 Pearlessence Sanitizing Wipes?

APPLY PRODUCT ALL OVER HANDS UNTIL DRY.CHILDREN SHOULD BE SUPERVISED AT ALL TIMES WHEN USING THIS PRODUCT.

Which are Pearlessence Sanitizing Wipes UNII Codes?

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

Which are Pearlessence Sanitizing Wipes 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".