NDC 73835-001

NaturAlixir

Alcohol

NaturAlixir is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by North Atlantic Chemicals And Technologies Llc. The primary component is Alcohol.

Product ID73835-001_7512967b-d117-4ee8-9a39-2ebf9eefea52
NDC73835-001
Product TypeHuman Otc Drug
Proprietary NameNaturAlixir
Generic NameAlcohol
Dosage FormGel
Route of AdministrationTOPICAL
Marketing Start Date2020-03-30
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart333A
Labeler NameNorth Atlantic Chemicals and Technologies LLC
Substance NameALCOHOL
Active Ingredient Strength70 mL/100mL
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 73835-001-02

59 mL in 1 BOTTLE (73835-001-02)
Marketing Start Date2020-03-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 73835-001-04 [73835000104]

NaturAlixir GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 73835-001-25 [73835000125]

NaturAlixir GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 73835-001-10 [73835000110]

NaturAlixir GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 73835-001-64 [73835000164]

NaturAlixir GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 73835-001-32 [73835000132]

NaturAlixir GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 73835-001-08 [73835000108]

NaturAlixir GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 73835-001-50 [73835000150]

NaturAlixir GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

NDC 73835-001-02 [73835000102]

NaturAlixir GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-03-30

Drug Details

Active Ingredients

IngredientStrength
ALCOHOL70 mL/100mL

OpenFDA Data

SPL SET ID:ee915031-d917-444e-83c5-fa694ee389ae
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 581662
  • NDC Crossover Matching brand name "NaturAlixir" or generic name "Alcohol"

    NDCBrand NameGeneric Name
    73835-001NaturAlixirNaturAlixir
    0363-0370Advanced Hand SanitizerAlcohol
    0363-9776Advanced Hand SanitizerAlcohol
    0363-0046AlcoholAlcohol
    0074-9857Alcohol - Hand SanitizerAlcohol
    0065-8000Alcohol Antiseptic 80%Alcohol
    0404-0122Antibacterialalcohol
    0395-0040Ethyl Rubbing AlcoholAlcohol
    0363-0968Hand SanitizerALCOHOL
    0219-2020Humphreys Alcoholado MaravillaALCOHOL
    0404-5988Instant Hand Sanitizeralcohol
    0295-9025Nozin Nasal SanitizerAlcohol
    0362-6000SeptoSanAlcohol
    0362-6001SeptoSanAlcohol
    0362-6002SeptoSanAlcohol
    0064-1050TRISEPTINALCOHOL
    0363-1305WalgreensAlcohol
    0363-1306WalgreensAlcohol
    0363-1307WalgreensAlcohol
    0363-1308WalgreensAlcohol
    0363-1309WalgreensAlcohol
    0363-0969Walgreens Advanced Hand Sanitizer Citrus ScentAlcohol
    0363-9005Walgreens Advanced Hand Sanitizer Made with Plant-Based Ethyl AlcoholAlcohol
    0363-9003Walgreens Advanced Hand Sanitizer with Aloe and Vitamin EAlcohol
    0363-0967WALGREENS ADVANCED HAND SANITIZER WITH FRESH SCENTALCOHOL
    0363-9004Walgreens Advanced Hand Sanitizer with Vitamin EAlcohol
    0363-9008Walgreens Advanced Hand Sanitizer with Vitamin EAlcohol
    0363-9006Walgreens Hand Sanitizer Coastal Breeze ScentAlcohol
    0363-9007Walgreens Hand Sanitizer Crisp Apple ScentAlcohol

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.