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

Avovenzone, Homosalate, Octisalate, Octocrylene, And Oxybenzone

NDC Product Code 13630-0086

NDC Code: 13630-0086

Proprietary Name: Australian Gold Broad Spectrum Spf 30 With Invisidry Technology What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Avovenzone, Homosalate, Octisalate, Octocrylene, And Oxybenzone What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 13630 - Prime Packaging, Inc.
    • 13630-0086 - Australian Gold

NDC 13630-0086-4

Package Description: 177 mL in 1 CAN

NDC Product Information

Australian Gold Broad Spectrum Spf 30 With Invisidry Technology with NDC 13630-0086 is a a human over the counter drug product labeled by Prime Packaging, Inc.. The generic name of Australian Gold Broad Spectrum Spf 30 With Invisidry Technology is avovenzone, homosalate, octisalate, octocrylene, and oxybenzone. The product's dosage form is aerosol, spray and is administered via topical form.

Labeler Name: Prime Packaging, Inc.

Dosage Form: Aerosol, Spray - An aerosol product which utilizes a compressed gas as the propellant to provide the force necessary to expel the product as a wet spray; it is applicable to solutions of medicinal agents in aqueous solvents.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Australian Gold Broad Spectrum Spf 30 With Invisidry Technology Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • AVOBENZONE 25.8 mg/mL
  • HOMOSALATE 64.5 mg/mL
  • OCTISALATE 43 mg/mL
  • OCTOCRYLENE 23.7 mg/mL
  • OXYBENZONE 17.2 mg/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
  • DIETHYLHEXYL 2,6-NAPHTHALATE (UNII: I0DQJ7YGXM)
  • POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) (UNII: T9296U138P)
  • FD&C RED NO. 40 (UNII: WZB9127XOA)
  • DIBUTYL MALEATE (UNII: 4X371TMK9K)
  • ISOBORNYL ACRYLATE (UNII: IX0PRH184P)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • ACACIA SENEGAL FLOWER (UNII: 72P931MTC2)
  • KAKADU PLUM (UNII: 0ZQ1D2FDLI)
  • GREEN TEA LEAF (UNII: W2ZU1RY8B0)
  • COFFEA ARABICA SEED, ROASTED (UNII: 9H58JRT35E)
  • FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
  • WATER (UNII: 059QF0KO0R)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Prime Packaging, Inc.
Labeler Code: 13630
FDA Application Number: part352 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 10-22-2012 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2019 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.

Exclude Flag: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Australian Gold Broad Spectrum Spf 30 With Invisidry Technology Product Label Images

Australian Gold Broad Spectrum Spf 30 With Invisidry Technology Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients

Avobenzone 3%, Homosalate 7.5%, Octisalate 5%, Octocrylene 2.75%, and Oxybenzone 2 %

Purpose

Sunscreen

Uses

  • Helps prevent sunburnif used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Otc - When Using

When using this product keep out of eyes. Rinse with water to remove. Keep away from face to avoid breathing it. Content under pressure - do not puncture or incinerate. Do not store at temperatures above 120°F.

Otc - Stop Use

Stop use and ask a doctor if rash occurs.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • 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

Inactive Ingredients

Acacia Senegal Flower/Stem Extract, Blue 1 (Cl 42090), Camellia Sinensis (Green Tea) Leaf Extract, Coddea Arabica (Kona Coffee) Seed Extract, Diethylhexyl 2,6-Naphthalate, Fragrance (Parfum), Glycerin, Polyester-8, Propylene Glycol, Red-40 (Cl 16035), SD Alcohol 40-B (Alcohol Denat), Terminalia Ferdinandiana (Kakadu Plum) Fruit Extract, TocopherylAcetate, VA/Butyl Maleate/Isobomyl Acrylate Copolymer, Water (Aqua), Yellow 5 (Cl 19140)

Other Information

  • Protect this product from excesive heat and direct sunavoid spraying on fabrics, could cause discoloration

* Please review the disclaimer below.

Previous Code
13630-0085
Next Code
13630-0087