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  4. NDC Product Code: 76214-033 Goat Milk And Lavender Sun For Baby Spf 20 Pa Plus Plus

NDC 76214-033 Goat Milk And Lavender Sun For Baby Spf 20 Pa Plus Plus

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 76214-033?
  4. Goat Milk And Lavender Sun For Baby Spf 20 Pa Plus Plus 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:
76214-033
Proprietary Name:
Goat Milk And Lavender Sun For Baby Spf 20 Pa Plus Plus
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Skinfood Co., Ltd.
Labeler Code:
76214
Product Label ID:
3be777bd-9132-4a69-98de-12b62525ad2f
Start Marketing Date: [9]
03-01-2011
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 76214-033-01

Package Description: 70 mL in 1 BOTTLE

Product Details

What is NDC 76214-033?

The NDC code 76214-033 is assigned by the FDA to the product Goat Milk And Lavender Sun For Baby Spf 20 Pa Plus Plus which is product labeled by Skinfood Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 76214-033-01 70 ml in 1 bottle . 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 Goat Milk And Lavender Sun For Baby Spf 20 Pa Plus Plus?

Indication and usage:Use at the end of your daily skincare regimen.Apply liberally onto face and body before sun exposure avoiding the eye area.

Which are Goat Milk And Lavender Sun For Baby Spf 20 Pa Plus Plus UNII Codes?

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

Which are Goat Milk And Lavender Sun For Baby Spf 20 Pa Plus Plus 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".