Merci Handy Rainbowtiful Hand Sanitizer

Alcohol

Merci Handy Corporation
Human Otc Drug
NDC 72866-013

Merci Handy Rainbowtiful Hand Sanitizer also known as Alcohol is a human otc drug labeled by 'Merci Handy Corporation'. National Drug Code (NDC) number for Merci Handy Rainbowtiful Hand Sanitizer is 72866-013. This drug is available in dosage form of Kit. The names of the active, medicinal ingredients in Merci Handy Rainbowtiful Hand Sanitizer drug includes . The currest status of Merci Handy Rainbowtiful Hand Sanitizer drug is Active.

Drug Information:

Drug NDC:	72866-013
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name:	Merci Handy Rainbowtiful Hand Sanitizer
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type:	Human Otc Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary Name:	Alcohol
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Merci Handy Corporation
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Kit
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status:	Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Marketing Category:	OTC MONOGRAPH NOT FINAL
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (ANDA), BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
Marketing Start Date:	01 Jan, 2021
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	30 Jun, 2025
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
Application Number:	part333E
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
Listing Expiration Date:	19 Jun, 2026
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Manufacturer Name:	MERCI HANDY CORPORATION
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
RxCUI:	1039708
The RxNorm Concept Unique Identifier. RxCUI is a unique number that describes a semantic concept about the drug product, including its ingredients, strength, and dose forms.
Original Packager:	Yes
Whether or not the drug has been repackaged for distribution.
UPC:	3760277820585 3760277822442
UPC stands for Universal Product Code.
UNII:
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
72866-013-01	1 KIT in 1 KIT (72866-013-01) * 30 mL in 1 BOTTLE (72866-005-30) * 30 mL in 1 BOTTLE (72866-008-30) * 30 mL in 1 BOTTLE (72866-006-30) * 30 mL in 1 BOTTLE (72866-002-30) * 30 mL in 1 BOTTLE (72866-000-30) * 30 mL in 1 BOTTLE (72866-001-30) * 30 mL in 1 BOTTLE (72866-010-30) * 30 mL in 1 BOTTLE (72866-007-30)	01 Jan, 2021	30 Jun, 2025	No
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

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Purpose:

Purpose antiseptic

Product Elements:

Merci handy rainbowtiful hand sanitizer alcohol hand sanitizer, mystic fruits alcohol water aloe vera leaf glycerin propylene glycol carbomer interpolymer type a (allyl sucrose crosslinked) aminomethylpropanol mannitol microcrystalline cellulose sucrose corn .alpha.-tocopherol acetate maltodextrin hypromellose, unspecified potassium sorbate sodium benzoate limonene, (+)- .alpha.-hexylcinnamaldehyde fd&c blue no. 1 d&c red no. 33 ferric ferrocyanide alcohol alcohol hand sanitizer, namaste alcohol water aloe vera leaf glycerin propylene glycol carbomer interpolymer type a (allyl sucrose crosslinked) aminomethylpropanol mannitol microcrystalline cellulose sucrose corn .alpha.-tocopherol acetate maltodextrin hypromellose, unspecified potassium sorbate sodium benzoate linalool, (+/-)- limonene, (+)- ferric ferrocyanide d&c red no. 33 d&c red no. 30 fd&c blue no. 1 alcohol alcohol hand sanitizer, coco rico alcohol water aloe vera leaf glycerin propylene glycol carbomer interpolymer type a (allyl sucrose crosslinked) aminomethylpropanol mannitol microcrystalline cellulose sucrose corn .alpha.-tocopherol acetate maltodextrin hypromellose, unspecified potassium sorbate sodium benzoate isomethyl-.alpha.-ionone benzyl salicylate coumarin geraniol limonene, (+)- fd&c blue no. 1 ferric ferrocyanide alcohol alcohol hand sanitizer, into the wild alcohol water aloe vera leaf glycerin propylene glycol carbomer interpolymer type a (allyl sucrose crosslinked) aminomethylpropanol mannitol microcrystalline cellulose sucrose corn .alpha.-tocopherol acetate maltodextrin hypromellose, unspecified potassium sorbate sodium benzoate limonene, (+)- citral fd&c yellow no. 5 chromic oxide fd&c blue no. 1 alcohol alcohol hand sanitizer, hello sunshine alcohol .alpha.-hexylcinnamaldehyde benzyl salicylate isomethyl-.alpha.-ionone .alpha.-amylcinnamyl alcohol fd&c yellow no. 5 fd&c red no. 4 ferric oxide red alcohol alcohol water aloe vera leaf glycerin propylene glycol carbomer interpolymer type a (allyl sucrose crosslinked) aminomethylpropanol mannitol microcrystalline cellulose sucrose corn .alpha.-tocopherol acetate maltodextrin hypromellose, unspecified potassium sorbate sodium benzoate .alpha.-amylcinnamaldehyde hand sanitizer, dolce vita alcohol water aloe vera leaf glycerin propylene glycol carbomer interpolymer type a (allyl sucrose crosslinked) aminomethylpropanol mannitol microcrystalline cellulose sucrose corn .alpha.-tocopherol acetate maltodextrin hypromellose, unspecified potassium sorbate sodium benzoate benzyl salicylate linalool, (+/-)- geraniol .beta.-citronellol, (r)- limonene, (+)- fd&c yellow no. 5 fd&c red no. 4 ferric oxide red alcohol alcohol hand sanitizer cherie cherry alcohol water aloe vera leaf glycerin propylene glycol carbomer interpolymer type a (allyl sucrose crosslinked) aminomethylpropanol mannitol microcrystalline cellulose sucrose corn .alpha.-tocopherol acetate maltodextrin hypromellose, unspecified potassium sorbate sodium benzoate eugenol coumarin isoeugenol limonene, (+)- fd&c red no. 4 d&c red no. 33 d&c red no. 30 alcohol alcohol hand sanitizer, flower power alcohol water aloe vera leaf glycerin propylene glycol carbomer interpolymer type a (allyl sucrose crosslinked) aminomethylpropanol mannitol microcrystalline cellulose sucrose corn .alpha.-tocopherol acetate maltodextrin hypromellose, unspecified potassium sorbate sodium benzoate .alpha.-amylcinnamaldehyde benzyl salicylate isomethyl-.alpha.-ionone limonene, (+)- d&c red no. 33 d&c red no. 30 alcohol alcohol

Indications and Usage:

Use for handwashing to decrease bacteria on the skin

Warnings:

Warnings for external use only. flammable, keep away from fire or flame. do not use in the eyes. in case of contact, flush eyes with water. stop use and ask a doctor if irritation and redness develop condition persists for more than 72 hours keep out of reach of children. if swallowed, get medical help or contact a poison control center right away.

Do Not Use:

Dosage and Administration:

Directions wet hands thoroughly with product and allow to dry without wiping

Stop Use:

Stop use and ask a doctor if irritation and redness develop condition persists for more than 72 hours

Package Label Principal Display Panel:

Package labeling:kit kit

Package labeling: mystic fruits label7

Package labeling: namaste box

Package labeling: coco rico rico

Package labeling:into the wild label2

Package labeling:hello sunshine label3

Package labeling:dolce vita label4

Package labeling:cherie cherry label5

Package labeling:flower power label6

Further Questions:

Questions or comments? (646)-358-3432

Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.