NDC 76598-002

Organic Antiseptic Gel

Alcohol

Organic Antiseptic Gel is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Bioagaves De La Costa, S.a. De C.v.. The primary component is Alcohol.

Product ID76598-002_a40f5348-5453-f910-e053-2995a90a8e90
NDC76598-002
Product TypeHuman Otc Drug
Proprietary NameOrganic Antiseptic Gel
Generic NameAlcohol
Dosage FormGel
Route of AdministrationTOPICAL
Marketing Start Date2020-04-24
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart333A
Labeler NameBioagaves de la Costa, S.A. de C.V.
Substance NameALCOHOL
Active Ingredient Strength80 mL/100mL
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 76598-002-01

250 mL in 1 BOTTLE (76598-002-01)
Marketing Start Date2020-04-24
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 76598-002-02 [76598000202]

Organic Antiseptic Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-24

NDC 76598-002-09 [76598000209]

Organic Antiseptic Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-24

NDC 76598-002-06 [76598000206]

Organic Antiseptic Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-24

NDC 76598-002-05 [76598000205]

Organic Antiseptic Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-24

NDC 76598-002-04 [76598000204]

Organic Antiseptic Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-24

NDC 76598-002-01 [76598000201]

Organic Antiseptic Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-24

NDC 76598-002-07 [76598000207]

Organic Antiseptic Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-24

NDC 76598-002-08 [76598000208]

Organic Antiseptic Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-24

NDC 76598-002-03 [76598000203]

Organic Antiseptic Gel GEL
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-24

Drug Details

Active Ingredients

IngredientStrength
ALCOHOL80 mL/100mL

OpenFDA Data

SPL SET ID:a40f5348-5452-f910-e053-2995a90a8e90
Manufacturer
UNII

NDC Crossover Matching brand name "Organic Antiseptic Gel" or generic name "Alcohol"

NDCBrand NameGeneric Name
76598-002Organic Antiseptic GelOrganic Antiseptic Gel
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.