Hand Recovery

Manufacturer: Derma Glove | RWM technologies Inc.
Effective date: 2025-11-14
Label type: HUMAN OTC DRUG LABEL
Version: 9
Source: full-release
Hydrated at: 2026-06-01 01:16:10

Label at a glance#

ProductHand Recovery

Active ingredientALCOHOL

Label structure12 sections

Contacts and useful links#

PhoneLabel contact1-888-300-1225

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 description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1809903	ethanol 70 % Topical Lotion	PSN	9
1809903	ethanol 0.7 ML/ML Topical Lotion	SCD	9
1809903	ethanol 70 % Topical Lotion	SY	9

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
70741-007-04	2023-07-31	C162847	48780-1	9d75b9d0-6e3e-f424-e053-dadaa90a57ce	90058ba8-e55d-4318-9fc5-8f0d25dfdd99
70741-007-04	2023-07-31	C162847	48780-1	9d75b9d0-6e3e-f424-e053-dadaa90a57ce	90058ba8-e55d-4318-9fc5-8f0d25dfdd99
70741-007-04	2022-01-28	C162847	48780-1	9d75b9d0-6e3e-f424-e053-dadaa90a57ce	90058ba8-e55d-4318-9fc5-8f0d25dfdd99
70741-007-04	2022-01-28	C162847	48780-1	9d75b9d0-6e3e-f424-e053-dadaa90a57ce	90058ba8-e55d-4318-9fc5-8f0d25dfdd99
70741-007-04	2020-05-22	C162847	48780-1	9d75b9d0-6e3e-f424-e053-dadaa90a57ce	90058ba8-e55d-4318-9fc5-8f0d25dfdd99
70741-007-04	2020-05-22	C162847	48780-1	9d75b9d0-6e3e-f424-e053-dadaa90a57ce	90058ba8-e55d-4318-9fc5-8f0d25dfdd99
70741-007-04	2020-01-31	C162847	48780-1	9d75b9d0-6e3e-f424-e053-dadaa90a57ce	90058ba8-e55d-4318-9fc5-8f0d25dfdd99
70741-007-04	2020-01-31	C162847	48780-1	9d75b9d0-6e3e-f424-e053-dadaa90a57ce	90058ba8-e55d-4318-9fc5-8f0d25dfdd99

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70741-007-04	Hand Recovery	236.8 mL in 1 PACKAGE	Lotion	236.8		9

Products#

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

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

Hand Recovery
Alcohol
Water

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
70741-007	70741-007-04

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
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
Water	059QF0KO0R	IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
6	2024-10-09	full-release	2026-06-01 00:24:03

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Hand Recovery	ALCOHOL	Derma Glove	90058ba8-e55d-4318-9fc5-8f0d25dfdd99	2025-11-14	Warnings	Exact identifier ndc (package): 70741-007-04 ndc (product): 70741-007 ndc11 (package): 70741000704 spl id: ce6a3b42-5dc8-4f62-9c9b-e24c3aed3be1 spl set id: 90058ba8-e55d-4318-9fc5-8f0d25dfdd99
Hand Recovery	ALCOHOL	Derma Glove	074a760f-9031-40c1-9867-95ef0345418d	2025-01-08	Warnings	Exact identifier ndc (product): 70741-007
Hand Recovery	ALCOHOL	Derma Glove	06f74478-57aa-4b8d-b888-55e1ee4fbd45	2024-10-09	Warnings	Exact identifier ndc (product): 70741-007
Hand Recovery	ALCOHOL	Derma Glove	e6cfe092-cb2c-441b-8897-98626c43bef8	2024-10-09	Warnings	Exact identifier ndc (product): 70741-007
Hand Recovery	ALCOHOL	Derma Glove	b4ff67d6-27d6-4d31-a708-9c2e8d4f0f3e	2024-10-09	Warnings	Exact identifier ndc (product): 70741-007
Hand Recovery	ALCOHOL	Derma Glove	d8705086-7209-4f13-bd54-604c90495f0a	2024-10-09	Warnings	Exact identifier ndc (product): 70741-007

Reported adverse events (FAERS/openFDA)#

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