1. Home
  2. Labeler Index
  3. Bona Fide Beauty Lab Ps Llc
  4. NDC Product Code: 72112-007 Be Sweet Spf 15 Tinted Full Hearts

NDC 72112-007 Be Sweet Spf 15 Tinted Full Hearts

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 72112-007?
  4. Be Sweet Spf 15 Tinted Full Hearts 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:
72112-007
Proprietary Name:
Be Sweet Spf 15 Tinted Full Hearts
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Bona Fide Beauty Lab Ps Llc
Labeler Code:
72112
Product Label ID:
21b2dc1a-13da-47a6-99d9-40dfed4d3598
Start Marketing Date: [9]
03-01-2018
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 72112-007?

The NDC code 72112-007 is assigned by the FDA to the product Be Sweet Spf 15 Tinted Full Hearts which is product labeled by Bona Fide Beauty Lab Ps Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72112-007-01 1 container in 1 carton / 2.7 g in 1 container. 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 Be Sweet Spf 15 Tinted Full Hearts?

Apply liberally 15 minutes before sun exposureUse a water resistant sunscreen if swimming or sweatingReapply at least every 2 hoursChildren under 6 months of age, ask a doctor prior to use

Which are Be Sweet Spf 15 Tinted Full Hearts UNII Codes?

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

Which are Be Sweet Spf 15 Tinted Full Hearts 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".