FDA.reportPublic FDA data

Hand Recovery

Manufacturer
Derma Glove | RWM Technologies Inc.
Effective date
2024-10-09
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-06-01 00:24:04

Label at a glance#

ProductHand Recovery
Active ingredientALCOHOL
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ethanol 70% v/v

OTC - PURPOSE SECTION

Antimicrobial

WARNINGS SECTION

For external use only. Flammable. Keep away from children.

OTC - WHEN USING SECTION

Do not use in or near eyes. In case of eye contact, rinse thoroughly with water.

OTC - STOP USE SECTION

If redness or irritation develop and persist for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Apply lotion directly onto body and rub with hands until dry. Product may be used on all skin surfaces. Children under 6 years of age should be supervised when using this product.

INDICATIONS & USAGE SECTION

Apply lotion directly onto body and rub with hands until dry. Product may be used on all skin surfaces. Children under 6 years of age should be supervised when using this product.

OTHER SAFETY INFORMATION

Do not store above 110oF (43oC). For additional information, see Safety Data Sheet (SDS).

INACTIVE INGREDIENT SECTION

Glycereth-18 (and) glycereth-18 ethylhexanoate, PEG-10 dimethicone, PEG-75 lanolin, ethylene glycol distearate, acrylate crosspolymer, 2-amino-2-methyl-1-propanol, water (aqua), PEG 1450, cocamide MEA

OTC - QUESTIONS SECTION

Call 1-888-300-1225, Monday through Friday 8:00AM to 5:00PM EST/EDT.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1809903ethanol 70 % Topical LotionPSN7
1809903ethanol 0.7 ML/ML Topical LotionSCD7
1809903ethanol 70 % Topical LotionSY7

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70741-007-012023-07-31C16284748780-19d75b9d0-6e41-f424-e053-dadaa90a57ceb4ff67d6-27d6-4d31-a708-9c2e8d4f0f3e
70741-007-012022-01-28C16284748780-19d75b9d0-6e41-f424-e053-dadaa90a57ceb4ff67d6-27d6-4d31-a708-9c2e8d4f0f3e
70741-007-012020-05-22C16284748780-19d75b9d0-6e41-f424-e053-dadaa90a57ceb4ff67d6-27d6-4d31-a708-9c2e8d4f0f3e
70741-007-012020-01-31C16284748780-19d75b9d0-6e41-f424-e053-dadaa90a57ceb4ff67d6-27d6-4d31-a708-9c2e8d4f0f3e

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70741-007-01Hand Recovery25 mL in 1 PACKAGELotion257

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70741-007HAND RECOVERY (ALCOHOL) LOTION [DERMA GLOVE]7Current NDC, Legacy NDC, 1 package rows20241011_b4ff67d6-27d6-4d31-a708-9c2e8d4f0f3e.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70741-00770741-007-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
Water059QF0KO0RIACT

Source Document#

Source XML · Source PDF

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 6 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Hand RecoveryALCOHOLDerma Glove90058ba8-e55d-4318-9fc5-8f0d25dfdd992025-11-14WarningsExact identifier
ndc (product): 70741-007
Hand RecoveryALCOHOLDerma Glove074a760f-9031-40c1-9867-95ef0345418d2025-01-08WarningsExact identifier
ndc (product): 70741-007
Hand RecoveryALCOHOLDerma Glove06f74478-57aa-4b8d-b888-55e1ee4fbd452024-10-09WarningsExact identifier
ndc (product): 70741-007
Hand RecoveryALCOHOLDerma Glovee6cfe092-cb2c-441b-8897-98626c43bef82024-10-09WarningsExact identifier
ndc (product): 70741-007
Hand RecoveryALCOHOLDerma Gloveb4ff67d6-27d6-4d31-a708-9c2e8d4f0f3e2024-10-09WarningsExact identifier
ndc (package): 70741-007-01
ndc (product): 70741-007
ndc11 (package): 70741000701
spl id: b504abc0-d55d-4200-87c3-f1cf7059893b
spl set id: b4ff67d6-27d6-4d31-a708-9c2e8d4f0f3e
Hand RecoveryALCOHOLDerma Gloved8705086-7209-4f13-bd54-604c90495f0a2024-10-09WarningsExact identifier
ndc (product): 70741-007

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.