NDC 70741-007

Hand Recovery

Alcohol

Hand Recovery is a Topical Lotion in the Human Otc Drug category. It is labeled and distributed by Derma Glove. The primary component is Alcohol.

Product ID70741-007_056dafe4-ee99-4e0d-b899-718e0d9697c3
NDC70741-007
Product TypeHuman Otc Drug
Proprietary NameHand Recovery
Generic NameAlcohol
Dosage FormLotion
Route of AdministrationTOPICAL
Marketing Start Date2017-01-06
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart333A
Labeler NameDerma Glove
Substance NameALCOHOL
Active Ingredient Strength70 mL/100mL
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 70741-007-06

947.2 mL in 1 PACKAGE (70741-007-06)
Marketing Start Date2017-01-06
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 70741-007-04 [70741000704]

Hand Recovery LOTION
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-01-06
Inactivation Date2020-01-31
Reactivation Date2020-05-22

NDC 70741-007-05 [70741000705]

Hand Recovery LOTION
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-01-06
Inactivation Date2020-01-31
Reactivation Date2020-05-22

NDC 70741-007-03 [70741000703]

Hand Recovery LOTION
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-01-06
Inactivation Date2020-01-31
Reactivation Date2020-05-22

NDC 70741-007-01 [70741000701]

Hand Recovery LOTION
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-01-06
Inactivation Date2020-01-31
Reactivation Date2020-05-22

NDC 70741-007-02 [70741000702]

Hand Recovery LOTION
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-01-06
Inactivation Date2020-01-31
Reactivation Date2020-05-22

NDC 70741-007-06 [70741000706]

Hand Recovery LOTION
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-01-06
Inactivation Date2020-01-31
Reactivation Date2020-05-22

Drug Details

Active Ingredients

IngredientStrength
ALCOHOL70 mL/100mL

OpenFDA Data

SPL SET ID:e6cfe092-cb2c-441b-8897-98626c43bef8
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1809903
  • NDC Crossover Matching brand name "Hand Recovery" or generic name "Alcohol"

    NDCBrand NameGeneric Name
    70741-007Hand RecoveryHand Recovery
    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

    Trademark Results [Hand Recovery]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    HAND RECOVERY
    HAND RECOVERY
    78125624 2880230 Live/Registered
    Crabtree & Evelyn, Ltd.
    2002-05-02

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