Humetec Rosemary Thyme Hand Sanitizer Mist

Humetec Rosemary Thyme Hand Sanitizer Mist by

Drug Labeling and Warnings

Humetec Rosemary Thyme Hand Sanitizer Mist by is a Otc medication manufactured, distributed, or labeled by Houston Medical Technologies LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

HUMETEC ROSEMARY THYME HAND SANITIZER MIST- alcohol liquid 
Houston Medical Technologies 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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Humetec Rosemary Thyme Hand Sanitizer Mist

Drug facts

Active ingredient

Ethyl Alcohol 70%

Purpose

Antimicrobial

Uses:

Hand Sanitizer to help reduce bacteria that potentially can cause disease.

Warnings:

For external use only. Flammable. Keep away from heat or flame. May discolor certain fabrics.

Do not use

In children under 2 months of age, and on open skin wounds.

When using this product

Keep out of eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if

irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach children

if swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Spray hands thoroughly with product and allow to dry without wiping
  • Supervise children under 6 years of age when using this product to avoid swallowing 
  • Do not use other than directed.

Other information

  • Store between 59°- 86° F (15° - 30°C)
  • Avoid freezing and excessive heat above 104°F (40°C)

Inactive ingredients

Water (aqua), Vegetable Glycerin, Fragrance.

Package Labeling:

Label2

HUMETEC ROSEMARY THYME HAND SANITIZER MIST 
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 80178-011
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 80178-011-0160 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product01/01/202210/31/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E01/01/202210/31/2023
Labeler - Houston Medical Technologies LLC (117519098)

Revised: 10/2022
Document Id: eb9901b8-7935-1e4a-e053-2a95a90a671a
Set id: ad0cc0a9-8dfb-4501-b5d6-1598ebf0977e
Version: 4
Effective Time: 20221022