HAND RELIEF- lotion lotion

Hand Relief by

Drug Labeling and Warnings

Hand Relief by is a Otc medication manufactured, distributed, or labeled by Derma Glove, RWM Technologies. 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.

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.

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.

OTHER SAFETY INFORMATION

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

INACTIVE INGREDIENT

Water (aqua), glycereth-18 (and) glycereth-18 ethylhexanoate, PEG 1450, PEG-10 dimethicone, ethylene glycol distearate, PEG 75 lanolin, cocamide MEA, retinyl palmitate (Vitamin A), magnesium ascorbyl phosphate (Vitamin C), d-l alpha tocopherol acetate (Vitamin E), acrylate crosspolymer, 2-amino-2-methyl-1-propanol, Cocos nucifera (Coconut oil), mentha piperita extract. 

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QUESTIONS

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

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PRINCIPAL DISPLAY PANEL

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INGREDIENTS AND APPEARANCE

HAND RELIEF 
lotion lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70741-012
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)	25 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70741-012-03	120 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	08/08/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	part333A	08/08/2023

Labeler - Derma Glove (962709569)

Registrant - Derma Glove (962709569)

Establishment
Name	Address	ID/FEI	Business Operations
RWM Technologies		626626969	manufacture(70741-012)