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  4. NDC Product Code: 54016-005 Baby Wipes

NDC 54016-005 Baby Wipes

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 54016-005?
  4. Baby Wipes Uses
  5. Active Ingredients UNII Codes
  6. 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:
54016-005
Proprietary Name:
Baby Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Jinhua Huihuang Non-woven Products Co., Ltd.
Labeler Code:
54016
Product Label ID:
aef07b16-36f6-19de-e053-2a95a90a5c70
Start Marketing Date: [9]
09-09-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 54016-005-01

Package Description: 60 PATCH in 1 PACKET / 6.85 mL in 1 PATCH

NDC Code 54016-005-02

Package Description: 1 PATCH in 1 PACKET / 6.85 mL in 1 PATCH

NDC Code 54016-005-03

Package Description: 10 PATCH in 1 PACKET / 6.85 mL in 1 PATCH

NDC Code 54016-005-04

Package Description: 15 PATCH in 1 PACKET / 6.85 mL in 1 PATCH

NDC Code 54016-005-05

Package Description: 20 PATCH in 1 PACKET / 6.85 mL in 1 PATCH

NDC Code 54016-005-06

Package Description: 25 PATCH in 1 PACKET / 6.85 mL in 1 PATCH

NDC Code 54016-005-07

Package Description: 30 PATCH in 1 PACKET / 6.85 mL in 1 PATCH

NDC Code 54016-005-08

Package Description: 40 PATCH in 1 PACKET / 6.85 mL in 1 PATCH

NDC Code 54016-005-09

Package Description: 50 PATCH in 1 PACKET / 6.85 mL in 1 PATCH

NDC Code 54016-005-10

Package Description: 80 PATCH in 1 PACKET / 6.85 mL in 1 PATCH

NDC Code 54016-005-11

Package Description: 90 PATCH in 1 PACKET / 6.85 mL in 1 PATCH

NDC Code 54016-005-12

Package Description: 100 PATCH in 1 PACKET / 6.85 mL in 1 PATCH

NDC Code 54016-005-13

Package Description: 120 PATCH in 1 PACKET / 6.85 mL in 1 PATCH

NDC Code 54016-005-14

Package Description: 150 PATCH in 1 PACKET / 6.85 mL in 1 PATCH

Product Details

What is NDC 54016-005?

The NDC code 54016-005 is assigned by the FDA to the product Baby Wipes which is product labeled by Jinhua Huihuang Non-woven Products Co., Ltd.. The product's dosage form is . The product is distributed in 14 packages with assigned NDC codes 54016-005-01 60 patch in 1 packet / 6.85 ml in 1 patch, 54016-005-02 1 patch in 1 packet / 6.85 ml in 1 patch, 54016-005-03 10 patch in 1 packet / 6.85 ml in 1 patch, 54016-005-04 15 patch in 1 packet / 6.85 ml in 1 patch, 54016-005-05 20 patch in 1 packet / 6.85 ml in 1 patch, 54016-005-06 25 patch in 1 packet / 6.85 ml in 1 patch, 54016-005-07 30 patch in 1 packet / 6.85 ml in 1 patch, 54016-005-08 40 patch in 1 packet / 6.85 ml in 1 patch, 54016-005-09 50 patch in 1 packet / 6.85 ml in 1 patch, 54016-005-10 80 patch in 1 packet / 6.85 ml in 1 patch, 54016-005-11 90 patch in 1 packet / 6.85 ml in 1 patch, 54016-005-12 100 patch in 1 packet / 6.85 ml in 1 patch, 54016-005-13 120 patch in 1 packet / 6.85 ml in 1 patch, 54016-005-14 150 patch in 1 packet / 6.85 ml in 1 patch. 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 Baby Wipes?

Wipe hands, discard properly in trash receptacle.Supervise children under 6 years of age when using this product to avoid swallowing.

Which are Baby Wipes UNII Codes?

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

Which are Baby 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:

* Please review the disclaimer below.

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".