Search by Drug Name or NDC

NDC 13630-0255-04 Australian Gold 16.42; 41.03; 16.42 g/mL; g/mL; g/mL Details

Australian Gold 16.42; 41.03; 16.42 g/mL; g/mL; g/mL

Australian Gold is a TOPICAL SPRAY in the HUMAN OTC DRUG category. It is labeled and distributed by Prime Packaging, Inc.. The primary component is AVOBENZONE; OCTISALATE; OCTOCRYLENE.

Product Information

NDC	13630-0255
Product ID	13630-0255_ece97025-156b-8ed3-e053-2995a90a3bff
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Australian Gold
Proprietary Name Suffix	Instant Bronzer Broad Spectrum SPF 15
Non-Proprietary Name	Avobenzone, Octisalate, Octocrylene
Product Type	HUMAN OTC DRUG
Dosage Form	SPRAY
Route	TOPICAL
Active Ingredient Strength	16.42; 41.03; 16.42
Active Ingredient Units	g/mL; g/mL; g/mL
Substance Name	AVOBENZONE; OCTISALATE; OCTOCRYLENE
Labeler Name	Prime Packaging, Inc.
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH FINAL
Application Number	M020
Listing Certified Through	2024-12-31

Package

Package Images

NDC 13630-0255-04 (13630025504)

Pricing Information	N/A
NDC Package Code	13630-0255-4
Billing NDC	13630025504
Package	207 mL in 1 CAN (13630-0255-4)
Marketing Start Date	2019-11-13
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL ece9637b-199d-6c2b-e053-2a95a90af94a Details

Active Ingredients

Avobenzone 2%

Octisalate 5%

Octocrylene 2%

Purpose

Sunscreen

Uses

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

Warnings

For external use only

Do not use on damaged or broken skin

When using this product keep away from face to avoid breathing it. Keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if rash occurs.

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

Flammable: Avoid fire, flame heat and smoking. Contents under pressure. Do not puncture or incinerate. Store at temperatures below 120°F (50°C).

Directions

shake well before use
apply liberally 15 minutes before sun exposure and rub into skin
hold container 4 to 6 inches from the skin to apply
do not spray directly into face. Spray on hands then apply to face
do not apply in windy conditions
use in a well-ventilated area
reapply:
after 80 minutes of swimming or sweating
immediately after towel drying
at least every 2 hours
Sun Protection Measures: Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF of 15 or higher and other sun protection measures including:
limit time in the sun, especially from 10 a.m. – 2 p.m.
wear long-sleeve shirts, pants, hats, and sunglasses
children under 6 months: Ask a doctor

Inactive ingredients

SD Alcohol 40-B [Alohol Denat.], Water/Aqua/Eau, VA/Butyl Maleate/Isobornyl Acrylate Copolymer, Fragrance, Polyester-8, Helianthus Annuus (Sunflower) Seed Oil, Tocopheryl Acetate, Yellow 5 (CI 19140), Glycerin, Aloe Barbadensis Leaf Extract, Red 40 (CI 16035), Melaleuca Alternifolia (Tea Tree) Leaf Oil, Blue 1 (CI 42090)

Other information

Protect this product from excessive heat and direct sun
May stain some fabrics or surfaces

Questions or comments?

Call toll free 1-885-LIV-GOLD (548-4653)

AUSTRALIAN GOLD INSTANT BRONZER 15 CONTINUOUS SPRAY SUNSCREEN

INGREDIENTS AND APPEARANCE

AUSTRALIAN GOLD INSTANT BRONZER BROAD SPECTRUM SPF 15

avobenzone, octisalate, octocrylene spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:13630-0255
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	16.42 g in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	41.03 g in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	16.42 g in 1 mL

Ingredient Name	Strength
Inactive Ingredients
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C RED NO. 40 (UNII: WZB9127XOA)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
SUNFLOWER OIL (UNII: 3W1JG795YI)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ISOBORNYL ACRYLATE (UNII: IX0PRH184P)
ALCOHOL (UNII: 3K9958V90M)
POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) (UNII: T9296U138P)
VINYL ACETATE (UNII: L9MK238N77)
DIBUTYL MALEATE (UNII: 4X371TMK9K)
TEA TREE OIL (UNII: VIF565UC2G)

Product Characteristics
Color	brown (Dark Amber)	Score
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:13630-0255-4	207 mL in 1 CAN; Type 0: Not a Combination Product	11/13/2019

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	M020	11/13/2019

Labeler - Prime Packaging, Inc. (805987059)

Registrant - Prime Packaging, Inc. (805987059)

Name	Address	ID/FEI	Business Operations
Establishment
Prime Enterprises, Inc.		101946028	manufacture(13630-0255) , analysis(13630-0255)

Name	Address	ID/FEI	Business Operations
Establishment
Prime Packaging, Inc.		805987059	label(13630-0255) , pack(13630-0255)

Revised: 11/2022

Document Id: ece97025-156b-8ed3-e053-2995a90a3bff

Set id: ece9637b-199d-6c2b-e053-2a95a90af94a

Version: 1

Effective Time: 20221107