VACATION SUPER- avobenzone homosalate octisalate octocrylene stick

Vacation Super by

Drug Labeling and Warnings

Vacation Super by is a Otc medication manufactured, distributed, or labeled by Vacation Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOSAGE & ADMINISTRATION

Apply liberally 15 minutes before sun exposure

Reapply at least every 2 hours

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

Stop use and ask a doctor if rash occurs

Inactives

Aloe Barbadensis Leaf Juice

Butyloctyl Salicylate

Calcium Sodium Phosphosilicate

Camellia Sinensis Leaf Extract

Caprylic/Capric Triglyceride

Ceramide NG

Ceramide NP

Cetyl Esters

Chlorella Vulgaris Extract

Cocos Nucifera (Coconut) Extract

Ethylhexylglycerin

Fragrance

Glycerin

Hyaluronic Acid

Lauroyl Lysine

Methylheptylglycerin

Musa Sapientum (Banana) Fruit Extract

Niacinamide

Olea Europaea (Olive) Fruit Oil

Polyglyceryl-10 Caprylate/Caprate

Polyurethane-35

Ricinus Communis (Castor) Seed Oil

Saccharomyces Ferment

Sodium Phytate

Sodium Stearate

Sorbitan Olivate

Tapioca Starch

Tocopherol

Tridecane

Trimethylpentanediol/Adipic Acid/Glycerin Crosspolymer

Undecane

Water

Indications and Usage

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

Keep out of reach of children

Keep out of reach of children

In case of ingestion, get medical help or contact a Poison Control Center right away

Purpose

Sunscreen

Vacation Super Stick SPF 45

INGREDIENTS AND APPEARANCE

VACATION SUPER 
avobenzone homosalate octisalate octocrylene stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80641-017
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	8.6 g  in 100 g
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	2.9 g  in 100 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	6.9 g  in 100 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	4.9 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80641-017-87	20 g in 1 APPLICATOR; Type 0: Not a Combination Product	03/12/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	03/12/2024

Labeler - Vacation Inc. (117644631)