NDC 13630-0086 Australian Gold Broad Spectrum Spf 30 With Invisidry Technology

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
13630-0086
Proprietary Name:
Australian Gold Broad Spectrum Spf 30 With Invisidry Technology
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
13630
Start Marketing Date: [9]
10-22-2012
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330)

Code Structure Chart

Product Details

What is NDC 13630-0086?

The NDC code 13630-0086 is assigned by the FDA to the product Australian Gold Broad Spectrum Spf 30 With Invisidry Technology which is product labeled by Prime Packaging, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 13630-0086-4 177 ml in 1 can . 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 Australian Gold Broad Spectrum Spf 30 With Invisidry Technology?

Spray liberally and spread evenly by hand 15 minutes before sun exposureChildren under 6 months: Ask a doctorHold container 4 to 6 inches from the skin to applyDo not spray directly into face. Spray hands then apply to face.Do not apply in windy conditions. Use in well ventilated areas.reapply:after 80 minutes of swimming or sweatingimmediately after towel dryingat least every 2 hours

Which are Australian Gold Broad Spectrum Spf 30 With Invisidry Technology UNII Codes?

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

Which are Australian Gold Broad Spectrum Spf 30 With Invisidry Technology 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".