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  4. NDC Product Code: 70630-1605 Bali Body Bb Cream Spf 15

NDC 70630-1605 Bali Body Bb Cream Spf 15

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 70630-1605?
  4. Bali Body Bb Cream Spf 15 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:
70630-1605
Proprietary Name:
Bali Body Bb Cream Spf 15
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Bali Body Pty Ltd
Labeler Code:
70630
Product Label ID:
9c6efc8e-f554-4982-892a-1c064073f15e
Start Marketing Date: [9]
06-08-2016
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 70630-1605-3

Package Description: 3 mL in 1 BOTTLE

Product Details

What is NDC 70630-1605?

The NDC code 70630-1605 is assigned by the FDA to the product Bali Body Bb Cream Spf 15 which is product labeled by Bali Body Pty Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70630-1605-3 3 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 Bali Body Bb Cream Spf 15?

Shake well before use. Apply liberaly 15 minutes before sun exposure.Children under 6 months old: Ask a doctor.Re-apply every 2 hours.Use water-resistant sunscreen if swimming or sweating.Store in cool dry place.

Which are Bali Body Bb Cream Spf 15 UNII Codes?

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

Which are Bali Body Bb Cream Spf 15 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".