NATURALIXIR- alcohol gel 
North Atlantic Chemicals and 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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NaturAlixir

Drug facts

Active ingredient(s)

Alcohol 70% w/w

Purpose

Antiseptic

Use(s) 

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

For external use only. Flammable. Keep away from heat or flame

Do not use

  • in children less than 2 months of age
  • on open skin wounds

When using this product keep out of eyes, ears and mouth. In case of contact with eye, rinse eyes thoroughly with water.

Stop use and see a doctor if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

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

Inactive ingredients Distilled Water, Lemon Orange Blossom (all natural) Fragrance Oil, Polyacrylate crosspolymer-6, Aloe Vera Leaf Juice, Vegetable Glycerin.

With Natural Ingredients

No Parabens, Aldehydes

No Animal-based Ingredients

Vegan

Packaging

IMAGE

NATURALIXIR 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73835-001
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)  
AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73835-001-0259 mL in 1 BOTTLE; Type 0: Not a Combination Product03/30/2020
2NDC:73835-001-04118 mL in 1 BOTTLE; Type 0: Not a Combination Product03/30/2020
3NDC:73835-001-08236 mL in 1 BOTTLE; Type 0: Not a Combination Product03/30/2020
4NDC:73835-001-32946 mL in 1 BOTTLE; Type 0: Not a Combination Product03/30/2020
5NDC:73835-001-641893 mL in 1 BOTTLE; Type 0: Not a Combination Product03/30/2020
6NDC:73835-001-103785 mL in 1 CONTAINER; Type 0: Not a Combination Product03/30/2020
7NDC:73835-001-259463 mL in 1 CONTAINER; Type 0: Not a Combination Product03/30/2020
8NDC:73835-001-5018927 mL in 1 CONTAINER; Type 0: Not a Combination Product03/30/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/30/2020
Labeler - North Atlantic Chemicals and Technologies LLC (081316806)
Establishment
NameAddressID/FEIBusiness Operations
North Atlantic Chemicals and Technologies LLC081316806manufacture(73835-001)

Revised: 3/2020
Document Id: 7512967b-d117-4ee8-9a39-2ebf9eefea52
Set id: ee915031-d917-444e-83c5-fa694ee389ae
Version: 1
Effective Time: 20200326
 
North Atlantic Chemicals and Technologies LLC