THYMES FRASIER FIR HAND SANITIZER- ethyl alcohol gel 
Bell International Laboratories, Inc

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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Thymes Frasier Fir Hand Sanitizer

Active Ingredient

Ethyl Alcohol 62% v/v

Purpose

Antiseptic

Use

To help reduce bacteria on the skin

Warnings

Flammable, keep away from heat and flame. For external use on the hands only. Avoid contact with eyes. If eye contact occurs, flush thoroughly with water. Avoid contact with broken skin. For Children under 6, use only under adult supervision.

Stop use and ask a doctor if ​​skin irritation develops

Keep out of reach of children. In case of accidental ingestion, seek medical assistance or contact a poison control center immediately.

Directions

Deposit a small amount in your palm and briskly rub hands together until dry.

Inactive Ingredients

Abies Sibirica Needle Oil, Aloe Barbadensis Leaf Juice, Aminomethyl Propanol, Carbomer, Fragrance, Glycerin, Helianthus Annuus (Sunflower) Seed Oil, Propanediol, Simmondsia Chinensis (Jojoba) Seed Oil, Tocopherol, Water

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THYMES FRASIER FIR HAND SANITIZER 
ethyl alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76150-339
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
TOCOPHEROL (UNII: R0ZB2556P8)  
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
JOJOBA OIL (UNII: 724GKU717M)  
PROPANEDIOL (UNII: 5965N8W85T)  
SUNFLOWER OIL (UNII: 3W1JG795YI)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
ABIES SIBIRICA LEAF OIL (UNII: XRY0V4VZKZ)  
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:76150-339-73251 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product08/01/2020
2NDC:76150-339-7254 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product07/01/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A08/01/2020
Labeler - Bell International Laboratories, Inc (967781555)

Revised: 4/2022
Document Id: dc270e36-d24a-d63e-e053-2995a90acc66
Set id: dc270e36-d249-d63e-e053-2995a90acc66
Version: 1
Effective Time: 20220408
 
Bell International Laboratories, Inc