SHIMMER OIL- avobenzone homosalate octisalate octocrylene oil

Shimmer Oil by

Drug Labeling and Warnings

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

Drug Details [pdf]

Dosage and Administration

Apply liberally 15 minutes before sun exposure

Reapply at least every 2 hours

Use a water resistant sunscreen if swimming or sweating

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 is rash occurs

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

Inactives

Argania Spinosa Kernel Oil, Bisabolol, Butyloctyl Salicylate, Butyrospermum Parkii (Shea) Oil, Calcium Sodium Borosilicate

Caprylic/Capric Triglyceride, Carthamus Tinctorius (Safflower) Seed Oil, Cocos Nucifera (Coconut) Oil, Dextrin Palmitate, Dimethicone, Ethyl Ferulate, Fragrance, Hyaluronic Acid, Iron Oxides, Mica, Musa Sapientum (Banana) Fruit Extract, Neopentyl Glycol, Diethylhexanoate, Palmitoyl Tripeptide-1, Sclerocarya Birrea Seed Oil, Simmondsia Chinensis (Jojoba) Seed Oil, Titanium Dioxide

Tocopherol, Trimethylpentanediol/Adipic Acid/Glycerin Crosspolymer

Vacation Shimmer Oil

INGREDIENTS AND APPEARANCE

SHIMMER OIL 
avobenzone homosalate octisalate octocrylene oil

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80641-015
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	2.9 g  in 100 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	8 g  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	4.9 g  in 100 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80641-015-15	86 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/07/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	03/07/2024

Labeler - Vacation Inc. (117644631)