Aloe Up SPF 50 C/S Sunscreen Aloe Vera

Aloe Up by

Drug Labeling and Warnings

Aloe Up by is a Otc medication manufactured, distributed, or labeled by Prime Packaging Inc, Prime Enterprises Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ALOE UP SPF 50 C/S SUNSCREEN WITH ALOE VERA- avobenzone, homosalate, octisalate, and octocrylene spray 
Prime Packaging Inc

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Aloe Up SPF 50 C/S Sunscreen Aloe Vera

Active Ingredients

Avobenzone 3%

Homosalate 15%

Octisalate 5%

Octocrylene 2.75%

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 out of eyes. Rinse with water to remove. Keep away from face to avoid breathing it. Contents under pressure - do not puncture or incinerate. Do not store at temperatures above 120ºF

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: Do not use near heat, flame or while smoking.

Directions

• Spray liberally and spread evenly by hand 15 minutes before sun exposure.
• 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

Aloe Barbadensis Extract, Cocos Nucifera (Coconut) Oil,Diethylhexyl 2,6-Naphthalate, Fragrance (Parfum), Mineral Oil (Paraffinum Liquidum), Polyester-8, SD Alcohol 40-B (Alcohol Denat.), VA/Butyl Maleate/Isobornyl Acrylate Copolymer

Other Information

• Protect this product from excessive heat and direct sun.
• Avoid spraying on fabrics - could cause discoloration.
• Store at 20ºC to 25ºC (68ºC to 77ºF)

Questions or comments?

Call toll free 1-800-950-2563

SPF 50 C/S Sunscreen Aloe Vera

ALOE UP  SPF 50 C/S SUNSCREEN WITH ALOE VERA
avobenzone, homosalate, octisalate, and octocrylene spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 13630-0225
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	127.05 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	42.35 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	23.29 mg  in 1 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	25.41 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
BENZYL ALCOHOL (UNII: LKG8494WBH)
COCONUT OIL (UNII: Q9L0O73W7L)
DIETHYLHEXYL 2,6-NAPHTHALATE (UNII: I0DQJ7YGXM)
MINERAL OIL (UNII: T5L8T28FGP)
POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) (UNII: T9296U138P)
ALCOHOL (UNII: 3K9958V90M)

Product Characteristics
Color	yellow (Light Yellow)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 13630-0225-4	183 mL in 1 CAN; Type 0: Not a Combination Product	05/22/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part352	05/22/2019

Labeler - Prime Packaging Inc (805987059)

Registrant - Prime Packaging Inc (805987059)

Establishment
Name	Address	ID/FEI	Business Operations
Prime Enterprises Inc		101946028	manufacture(13630-0225) , analysis(13630-0225)

Establishment
Name	Address	ID/FEI	Business Operations
Prime Packaging Inc		805987059	label(13630-0225) , pack(13630-0225)

Revised: 2/2022

Document Id: d71fd4b6-a84f-44fd-e053-2a95a90a0b60

34390-5

Set id: d71fd3e6-07b1-7ce4-e053-2a95a90a3cae

Version: 1

Effective Time: 20220203