NDC 51098-742 Hands First 4 In 1
NDC Product Code 51098-742
Proprietary Name: Hands First 4 In 1 What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name: What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
NDC Code Structure
- 51098 - Avadim Ii Llc
- 51098-742 - Hands First
NDC 51098-742-01
Package Description: 50 mL in 1 BOTTLE, PLASTIC
NDC 51098-742-02
Package Description: 360 mL in 1 BOTTLE, PLASTIC
NDC Product Information
Hands First 4 In 1 with NDC 51098-742 is a product labeled by Avadim Ii Llc. The generic name of Hands First 4 In 1 is . The product's dosage form is and is administered via form.
Dosage Form: -
Product Type: What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
Product Labeler Information
What is the Labeler Name?Name of Company corresponding to the labeler code segment of the Product NDC.
Labeler Name: Avadim Ii Llc
Labeler Code: 51098
Start Marketing Date: 08-01-2010 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: 12-31-2017 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 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. Values = ‘Y’ or ‘N’.
* Please review the disclaimer below.
Hands First 4 In 1 Product Label Images
Hands First 4 In 1 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
Allantoin 0.5%Benzalkonium Chloride 0.13%
Otc - Purpose
Skin ProtectantAntimicrobialUse(s)For handwashing to decrease bacteria on the skinFor temporary protection of minor cuts, scrapes, burns, and chapped or cracked skinDirectionsUse as neededRemove cap and pump foam into palm of hand.Rub foam onto handsAllow to air dry
Warnings
For external use onlyKeep out of the reach of childrenDo not use in the eyesDo not use on deep or puncture wounds, animal bites, or serious burnsExtended use may increase risk of sunburn
Otc - Stop Use
Stop use and ask a doctor if condition worsens or symptoms last more than seven days.
Inactive Ingredient
Purified Water, tego-betaine, aloe vera, dimethicone, *collodial silver, glycolic acid, potassium hydroxide, EDTA, phenoxyethanol, isobutyl paraben, propyl paraben, ethyl paraben, butyl paraben, methyl paraben*Preservative only .1%
* Please review the disclaimer below.