NDC 72866-030 Holiday Dust Set

Alcohol

NDC Product Code 72866-030

NDC 72866-030-01

Package Description: 1 KIT in 1 KIT * 30 mL in 1 BOTTLE (72866-032-01) * 30 mL in 1 BOTTLE (72866-033-01) * 30 mL in 1 BOTTLE (72866-031-01)

NDC Product Information

Holiday Dust Set with NDC 72866-030 is a a human over the counter drug product labeled by Merci Handy Corporation. The generic name of Holiday Dust Set is alcohol. The product's dosage form is kit and is administered via topical form.

Dosage Form: Kit - A packaged collection of related material.

Product Type: Human Otc Drug 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.

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)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
  • AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
  • MANNITOL (UNII: 3OWL53L36A)
  • MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
  • SUCROSE (UNII: C151H8M554)
  • CORN (UNII: 0N8672707O)
  • DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • MALTODEXTRIN (UNII: 7CVR7L4A2D)
  • HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
  • POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
  • SODIUM BENZOATE (UNII: OJ245FE5EU)
  • D&C RED NO. 30 (UNII: 2S42T2808B)
  • D&C RED NO. 33 (UNII: 9DBA0SBB0L)
  • WATER (UNII: 059QF0KO0R)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
  • AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
  • MANNITOL (UNII: 3OWL53L36A)
  • MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
  • SUCROSE (UNII: C151H8M554)
  • CORN (UNII: 0N8672707O)
  • DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • MALTODEXTRIN (UNII: 7CVR7L4A2D)
  • HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
  • POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
  • SODIUM BENZOATE (UNII: OJ245FE5EU)
  • BENZYL BENZOATE (UNII: N863NB338G)
  • COUMARIN (UNII: A4VZ22K1WT)
  • LIMONENE, (+)- (UNII: GFD7C86Q1W)
  • GERANIOL (UNII: L837108USY)
  • CHROMIC OXIDE (UNII: X5Z09SU859)
  • FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
  • WATER (UNII: 059QF0KO0R)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
  • AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
  • MANNITOL (UNII: 3OWL53L36A)
  • MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
  • SUCROSE (UNII: C151H8M554)
  • CORN (UNII: 0N8672707O)
  • DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • MALTODEXTRIN (UNII: 7CVR7L4A2D)
  • HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
  • POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
  • SODIUM BENZOATE (UNII: OJ245FE5EU)
  • FERRIC FERROCYANIDE (UNII: TLE294X33A)
  • D&C RED NO. 30 (UNII: 2S42T2808B)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
  • D&C RED NO. 33 (UNII: 9DBA0SBB0L)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

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

Labeler Name: Merci Handy Corporation
Labeler Code: 72866
FDA Application Number: part333E What is the FDA Application Number?
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.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/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.

Start Marketing Date: 09-20-2021 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: 12-31-2022 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: N - NO 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.

Holiday Dust Set 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

Active Ingredient

Alcohol 67%

Alcohol 67%

Alcohol 67%

Purpose

Antiseptic

Antiseptic

Antiseptic

Use

  • For handwashing to decrease bacteria on the skin

  • For handwashing to decrease bacteria on the skin

  • For handwashing to decrease bacteria on the skin

Warnings

For external use only. Flammable, keep away from fire or flame.

For external use only. Flammable, keep away from fire or flame.

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.

In the eyes. In case of contact, flush eyes with water.

In the eyes. In case of contact, flush eyes with water.

Stop Use And Ask A Doctor If

  • Irritation and redness developcondition persists for more than 72 hours

  • Irritation and redness developcondition persists for more than 72 hours

  • Irritation and redness developcondition 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.

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

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

Directions

Wet hands thoroughly with product and allow to dry without wiping

Wet hands thoroughly with product and allow to dry without wiping

Wet hands thoroughly with product and allow to dry without wiping

Other Information

Store at a temperature below 110° F (43° C)

Store at a temperature below 110° F (43° C)

Store at a temperature below 110° F (43° C)

Inactive Ingredients

Aqua (Water), Parfum (Fragrance), Aloe Barbadensis Leaf Juice Powder, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Mannitol, Microcrystalline Cellulose, Sucrose, Zea Mays (Corn) Starch, Denatonium Benzoate, Tocopheryl Acetate, Maltodextrin, Hydroxypropyl Methylcellulose, Potassium Sorbate, Sodium Benzoate, D&C Red No. 30, D&C Red No. 33.

Aqua (Water), Parfum (Fragrance), Aloe Barbadensis Leaf Juice Powder, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Mannitol, Microcrystalline Cellulose, Sucrose, Zea Mays (Corn) Starch, Denatonium Benzoate, Tocopheryl Acetate, Maltodextrin, Hydroxypropyl Methylcellulose, Potassium Sorbate, Sodium Benzoate, Benzyl Benzoate, Coumarin, Limonene, Geraniol, Chromium Oxide Greens, FD&C Yellow No. 5, FD&C Blue No. 1.

Aqua (Water), Parfum (Fragrance), Aloe Barbadensis Leaf Juice Powder, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Mannitol, Microcrystalline Cellulose, Sucrose, Zea Mays (Corn) Starch, Denatonium Benzoate, Tocopheryl Acetate, Maltodextrin, Hydroxypropyl Methylcellulose, Potassium Sorbate, Sodium Benzoate, Ferric Ferrocyanide, D&C Red No. 30, FD&C Blue No. 1, D&C Red No. 33.

* Please review the disclaimer below.