OTC Medication Information: Hand

HAND- alcohol lotion
Derma Glove

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Ethanol 70% v/v

Antimicrobial

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

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

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

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

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.

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.

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

Water (aqua), glycereth-18 (and) glycereth-18 ethylhexanoate, cocamide MEA, PEG 75 lanolin, PEG 10 dimethicone, PEG 1450, ethylene glycol distearate, Vitamin A (retinyl palmitate), Vitamin E (d-l alpha tocopherol acetate), Vitamin C (magnesium ascorbyl phosphate), acrylate crosspolymer, Diospyros kaki extract, 2-amino-2-methyl-1-propanol, FD&C Red #40, FD&C Blue #1.

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

image description
(click image for full-size original)

HAND
lotion lotion
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:70741-006
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Alcohol (ALCOHOL) Alcohol 70 mL in 100 mL
Inactive Ingredients
Ingredient Name Strength
Water 20 mL in 100 mL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:70741-006-04 236.8 mL in 1 BOTTLE, PUMP None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333A 09/14/2016
Labeler — Derma Glove (962709569)
Registrant — Derma Glove (962709569)
Establishment
Name Address ID/FEI Operations
RWM Technologies Inc. 626626969 manufacture (70741-006)

Revised: 05/2020 Derma Glove

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Medication Sections

Medication Information by RSS

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Terms of Use | Copyright © 2021. All Rights Reserved.