NDC 70741-007 Hand Recovery

NDC Product Code 70741-007

NDC 70741-007-01

Package Description: 25 mL in 1 PACKAGE

NDC 70741-007-02

Package Description: 40 mL in 1 PACKAGE

NDC 70741-007-03

Package Description: 75 mL in 1 PACKAGE

NDC 70741-007-04

Package Description: 236.8 mL in 1 PACKAGE

NDC 70741-007-05

Package Description: 473.6 mL in 1 PACKAGE

NDC 70741-007-06

Package Description: 947.2 mL in 1 PACKAGE

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Hand Recovery with NDC 70741-007 is product labeled by Derma Glove. The product's dosage form is and is administered via form.

RxNorm Crosswalk

What is RxNorm?
RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) (RxCUI) to each NDC.

The RxNorm Crosswalk for this NDC code indicates a single concept unique identifier (RXCUI) is associated with this product:


Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • WATER (UNII: 059QF0KO0R)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Derma Glove
Labeler Code: 70741
Start Marketing Date: 01-06-2017 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2021 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Hand Recovery Product Label Images

Hand Recovery Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Otc - Active Ingredient

Ethanol 70% v/v

Otc - Purpose

Antimicrobial

Warnings

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

Otc - When Using

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

Otc - Stop Use

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

Otc - 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

Otc - Questions

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

* Please review the disclaimer below.