THYMES FRASIER FIR HAND SANITIZER- ethyl alcohol gel

Thymes Frasier Fir Hand Sanitizer by

Drug Labeling and Warnings

Thymes Frasier Fir Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Bell International Laboratories, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

THYMES FRASIER FIR HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76150-339
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76150-339-73	251 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	08/01/2020
2	NDC: 76150-339-72	54 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	07/01/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/01/2020

Labeler - Bell International Laboratories, Inc (967781555)