NDC 69366-301

Hand Sanitizer Orange with aloe

62% Hand Sanitizer Spray

Hand Sanitizer Orange with aloe is a Topical Spray in the Human Otc Drug category. It is labeled and distributed by The Honest Company, Inc.. The primary component is Alcohol.

Product ID69366-301_33ac19ad-81d0-3ee3-e054-00144ff88e88
NDC69366-301
Product TypeHuman Otc Drug
Proprietary NameHand Sanitizer Orange with aloe
Generic Name62% Hand Sanitizer Spray
Dosage FormSpray
Route of AdministrationTOPICAL
Marketing Start Date2016-01-01
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart333A
Labeler NameThe Honest Company, Inc.
Substance NameALCOHOL
Active Ingredient Strength62 mL/100mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 69366-301-04

60 mL in 1 BOTTLE, PLASTIC (69366-301-04)
Marketing Start Date2016-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 69366-301-04 [69366030104]

Hand Sanitizer Orange with aloe SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-01

Drug Details

Active Ingredients

IngredientStrength
ALCOHOL62 mL/100mL

OpenFDA Data

SPL SET ID:33ac19ad-81cf-3ee3-e054-00144ff88e88
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1020364
  • NDC Crossover Matching brand name "Hand Sanitizer Orange with aloe" or generic name "62% Hand Sanitizer Spray"

    NDCBrand NameGeneric Name
    69366-307Hand Sanitizer Orange with aloeHand Sanitizer Orange with aloe
    69366-304hand sanitizer orange with aloehand sanitizer orange with aloe
    69366-301Hand Sanitizer62% Hand Sanitizer Spray
    69366-302Hand Sanitizer62% Hand Sanitizer Spray

    Trademark Results [Hand Sanitizer]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    HAND SANITIZER
    HAND SANITIZER
    88958909 not registered Live/Pending
    MAISON BLANCHE, LLC
    2020-06-10

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