VACATION INSTANT BROWNING- avobenzone octisalate octocrylene lotion

Vacation Instant Browning by

Drug Labeling and Warnings

Vacation Instant Browning 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 water-resistent 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 reach of eyes. Rinse with water to remove.

Stop use and ask a doctor if rash occurs

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

Inactives

OCTISALATE, OCTOCRYLENE, ACETYL L-TYROSINE, LEVOMENOL, MAGNESIUM STEARATE, OCTYLDODECYL OLEATE, WATER, C13-15 ALKANE, PROPANEDIOL, COCOA BUTTER, TOCOPHEROL, VANILLA PLANIFOLIA OIL, DOCOSANOL, DECYL GLUCOSIDE, SODIUM METABISULFITE, PORPHYRIDIUM PURPUREUM, ALCOHOL, BUTYLOCTYL SALICYLATE, BUTYROSPERMUM PARKII (SHEA) BUTTER UNSAPONIFIABLES, CAPRYLHYDROXAMIC ACID, CAPRYLYL GLYCOL, CETOSTEARYL ALCOHOL, CETYL ALCOHOL, CITRIC ACID MONOHYDRATE, COCO GLUCOSIDE, ARABICA COFFEE OIL, EUROPEAN HAZELNUT OIL, DIHYDROXYACETONE, DIMETHICONE, ETHYLENE BRASSYLATE, ETHYL FERULATE, GLYCERIN, FERRIC OXIDE RED, LAURYL GLUCOSIDE, PASSIFLORA EDULIS SEED OIL, CHASTE TREE

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 agin caused by the sun.

Keep out of reach of children

Keep out of reach of childen

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

Purpose

Sunscreen

Vacation Browning Lotion

INGREDIENTS AND APPEARANCE

VACATION INSTANT BROWNING 
avobenzone octisalate octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80641-521
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	9.5 g  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	4.9 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ACETYL L-TYROSINE (UNII: DA8G610ZO5)
LEVOMENOL (UNII: 24WE03BX2T)
MAGNESIUM STEARATE (UNII: 70097M6I30)
OCTYLDODECYL OLEATE (UNII: MCA43PK7MH)
WATER (UNII: 059QF0KO0R)
C13-15 ALKANE (UNII: 114P5I43UJ)
PROPANEDIOL (UNII: 5965N8W85T)
COCOA BUTTER (UNII: 512OYT1CRR)
TOCOPHEROL (UNII: R0ZB2556P8)
VANILLA PLANIFOLIA OIL (UNII: 0A3F415158)
DOCOSANOL (UNII: 9G1OE216XY)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
SODIUM METABISULFITE (UNII: 4VON5FNS3C)
PORPHYRIDIUM PURPUREUM (UNII: K2P8K2558N)
ALCOHOL (UNII: 3K9958V90M)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
BUTYROSPERMUM PARKII (SHEA) BUTTER UNSAPONIFIABLES (UNII: 0C9AC7D6XU)
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
CETYL ALCOHOL (UNII: 936JST6JCN)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
COCO GLUCOSIDE (UNII: ICS790225B)
ARABICA COFFEE OIL (UNII: IK55HKE887)
EUROPEAN HAZELNUT OIL (UNII: 8RQ2839AVG)
DIHYDROXYACETONE (UNII: O10DDW6JOO)
DIMETHICONE (UNII: 92RU3N3Y1O)
ETHYLENE BRASSYLATE (UNII: 9A87HC7ROD)
ETHYL FERULATE (UNII: 5B8915UELW)
GLYCERIN (UNII: PDC6A3C0OX)
FERRIC OXIDE RED (UNII: 1K09F3G675)
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
PASSIFLORA EDULIS SEED OIL (UNII: F3VOA31UHQ)
CHASTE TREE (UNII: 433OSF3U8A)
SODIUM GLUCONATE (UNII: R6Q3791S76)
APRICOT SEED OIL (UNII: 54JB35T06A)
SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)
TRIHEPTANOIN (UNII: 2P6O7CFW5K)
XANTHAN GUM (UNII: TTV12P4NEE)
METHYL DIHYDROABIETATE (UNII: 7666FJ0J9F)
ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)
CARROT SEED OIL (UNII: 595AO13F11)
ERYTHRULOSE, D- (UNII: 09058VOU0Z)
HYALURONIC ACID (UNII: S270N0TRQY)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80641-521-10	148 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/06/2024
2	NDC: 80641-521-80	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/06/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	03/06/2024

Labeler - Vacation Inc. (117644631)