HAND RECOVERY- alcohol lotion

Hand Recovery by

Drug Labeling and Warnings

Hand Recovery by is a Otc medication manufactured, distributed, or labeled by Derma Glove, Mid Lab Incorporated. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Ethanol 70% v/v

PURPOSE

Antimicrobial

WARNINGS

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

WHEN USING

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

STOP USE

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

KEEP OUT OF REACH OF CHILDREN

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

DOSAGE & ADMINISTRATION

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

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

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

QUESTIONS

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HAND RECOVERY 
alcohol lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70741-007
Route of Administration	Topical

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)	20 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70741-007-04	236.8 mL in 1 PACKAGE; Type 0: Not a Combination Product	01/06/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/06/2017

Labeler - Derma Glove (962709569)

Registrant - Derma Glove (962709569)

Establishment
Name	Address	ID/FEI	Business Operations
Mid Lab Incorporated		047371463	manufacture(70741-007)