VACATION INSTANT BROWNING- avobenzone octisalate octocrylene lotion 
Vacation Inc.

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Vacation Instant Browning Lotion

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

Browning Lotion 5oz

VACATION INSTANT BROWNING 
avobenzone octisalate octocrylene lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80641-521
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE2.9 g  in 100 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE9.5 g  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE4.9 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:80641-521-10148 mL in 1 BOTTLE; Type 0: Not a Combination Product03/06/2024
2NDC:80641-521-8030 mL in 1 BOTTLE; Type 0: Not a Combination Product03/06/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02003/06/2024
Labeler - Vacation Inc. (117644631)

Revised: 3/2024
Document Id: 13028f61-3f63-22cc-e063-6394a90a6bf1
Set id: 13028f61-3f62-22cc-e063-6394a90a6bf1
Version: 1
Effective Time: 20240306
 
Vacation Inc.