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  4. NDC Product Code: 57691-161 01 Moisture Foundation Spf 15

NDC 57691-161 01 Moisture Foundation Spf 15

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 57691-161?
  5. 01 Moisture Foundation Spf 15 Uses
  6. Active 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:
57691-161
Proprietary Name:
01 Moisture Foundation Spf 15
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
The Body Shop Wake Forest
Labeler Code:
57691
Product Label ID:
90323a05-4f28-4dbd-bd37-26ce0826374d
Start Marketing Date: [9]
09-06-2009
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
BROWN (C48332)

Product Packages

NDC Code 57691-161-30

Package Description: 30 mL in 1 BOTTLE, PUMP

Product Details

What is NDC 57691-161?

The NDC code 57691-161 is assigned by the FDA to the product 01 Moisture Foundation Spf 15 which is product labeled by The Body Shop Wake Forest. The product's dosage form is . The product is distributed in a single package with assigned NDC code 57691-161-30 30 ml in 1 bottle, pump . 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 01 Moisture Foundation Spf 15?

Apply evenly before sun exposure and as needed.for use in children under 6 months old, ask a doctor.shake well before use.

Which are 01 Moisture Foundation Spf 15 UNII Codes?

The UNII codes for the active 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".