TROPICAL FOREST HAND SANITIZER- alcohol gel 
REACTION RETAIL LLC

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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Tropical Forest Hand Sanitizer

Drug Facts

Active Ingredient:

Ethyl Alcohol 75%

Antiseptic

Uses:

Hand sanitizer to help decrease bacteria on the skin.

Warnings:

For external use only.

Flammable. Keep away from fire or flame.

Stop use and ask doctor if

irritation or rash appears and lasts.

Keep out of reach of children.

If swallowed, get medical help or contact a doctor right away.

Directions:

Squirt as needed into your palms and thoroughly spread on both hands. Rub into skin until dry.

Other Information:

Store below 118°F

Inactive Ingredients:

Aqua (Water), Glycerin, Propylene Glycol, Aloe Barbadensis Leaf Juice, Parfum (Fragrance), Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Benzophenone-3, Triethanolamine, Citric Acid, Potassium Sorbate, Sodium Benzoate, Sucrose, Zea Mays (Corn) Starch, Hydroxypropyl Methylcellulose, Polyvinyl Alcohol, Hexyl Cinnamal, Linalool, Citronello, Limonene, Coumarin, Geraniol, Benzyl Benzoate, CL 77267 (D&C Black No.3), CI 19140(FD&C Yellow No.5), CI42090 (FD&C Blue No.1).

Package Labeling:

Bottle

TROPICAL FOREST HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80026-011
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.75 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
OXYBENZONE (UNII: 95OOS7VE0Y)  
TROLAMINE (UNII: 9O3K93S3TK)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SUCROSE (UNII: C151H8M554)  
STARCH, CORN (UNII: O8232NY3SJ)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)  
.ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)  
LINALOOL, (+/-)- (UNII: D81QY6I88E)  
.BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)  
LIMONENE OXIDE, (+)- (UNII: 278IM94GXB)  
COUMARIN (UNII: A4VZ22K1WT)  
GERANIOL (UNII: L837108USY)  
BENZYL BENZOATE (UNII: N863NB338G)  
D&C BLACK NO. 2 (UNII: 4XYU5U00C4)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:80026-011-3030 mL in 1 BOTTLE; Type 0: Not a Combination Product10/20/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E10/20/2020
Labeler - REACTION RETAIL LLC (968085212)

Revised: 10/2020
Document Id: b230323c-126c-ecfb-e053-2a95a90af3b3
Set id: b2303230-6a63-e83d-e053-2a95a90a6d59
Version: 1
Effective Time: 20201021
 
REACTION RETAIL LLC