NDC 10056-041 Artistry Skin Nutrition Hydrating Day

Avobenzone, Octisalate, Octocrylene

NDC Product Code 10056-041

NDC CODE: 10056-041

Proprietary Name: Artistry Skin Nutrition Hydrating Day 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: Avobenzone, Octisalate, Octocrylene 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

  • 10056 - Access Business Group Llc
    • 10056-041 - Artistry Skin Nutrition Hydrating Day

NDC 10056-041-00

Package Description: 1 TUBE in 1 CARTON > 50 g in 1 TUBE

NDC Product Information

Artistry Skin Nutrition Hydrating Day with NDC 10056-041 is a a human over the counter drug product labeled by Access Business Group Llc. The generic name of Artistry Skin Nutrition Hydrating Day is avobenzone, octisalate, octocrylene. The product's dosage form is lotion and is administered via topical form.

Labeler Name: Access Business Group Llc

Dosage Form: Lotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2

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.

Artistry Skin Nutrition Hydrating Day Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • AVOBENZONE 30 mg/g
  • OCTISALATE 50 mg/g
  • OCTOCRYLENE 70 mg/g

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)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • PROPANEDIOL (UNII: 5965N8W85T)
  • BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
  • CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • POLYSORBATE 80 (UNII: 6OZP39ZG8H)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • CHIA SEED OIL (UNII: MC2LH51BO7)
  • CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • CHLORPHENESIN (UNII: I670DAL4SZ)
  • ACEROLA (UNII: XDD2WEC9L5)
  • PENTYLENE GLYCOL (UNII: 50C1307PZG)
  • ALLANTOIN (UNII: 344S277G0Z)
  • CARNOSINE (UNII: 8HO6PVN24W)
  • GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
  • DIPROPYLENE GLYCOL (UNII: E107L85C40)
  • EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
  • ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
  • TOCOPHEROL (UNII: R0ZB2556P8)
  • SOYBEAN OIL (UNII: 241ATL177A)
  • MALTODEXTRIN (UNII: 7CVR7L4A2D)
  • CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
  • PENTADECALACTONE (UNII: OK17S3S98K)
  • CARRAGEENAN (UNII: 5C69YCD2YJ)
  • POMEGRANATE (UNII: 56687D1Z4D)
  • ZINC PIDOLATE (UNII: C32PQ86DH4)
  • RUBUS FRUTICOSUS LEAF (UNII: YQ2S06L8S9)
  • CERAMIDE NP (UNII: 4370DF050B)
  • SEA SALT (UNII: 87GE52P74G)
  • .BETA.-SITOSTEROL (UNII: S347WMO6M4)
  • HYALURONATE SODIUM (UNII: YSE9PPT4TH)
  • EVENING PRIMROSE OIL (UNII: 3Q9L08K71N)
  • PERILLA FRUTESCENS SEED OIL (UNII: 322MS57V7Z)
  • SUNFLOWER OIL (UNII: 3W1JG795YI)
  • BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)

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: Access Business Group Llc
Labeler Code: 10056
FDA Application Number: part352 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: 04-04-2021 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.

Artistry Skin Nutrition Hydrating Day Product Label Images

Artistry Skin Nutrition Hydrating Day 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 Ingredients (W/W)

Avobenzone 3%


Octisalate 5%


Octocrylene 7%

Purpose

Sunscreen

Uses

Helps prevent sunburn

Warnings

For external use only

Do Not Use

On broken or damaged skin

When Using This Product

Keep out of eyes. Rinse with water to remove.

Stop Use And Ask A Doctor

If rash occurs

Keep Out Of Reach Of Children.

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

Directions

  • For sunscreen useApply liberally 15 minutes before sun exposureUse a water resistant sunscreen if swimming or sweating or washingReapply at least every 2 hoursChildren under 6 months: ask a doctor

Other Information

  • Protect this product from excessive heat and direct sun

Inactive Ingredients

Water, dimethicone, propanediol, butyloctyl salicylate, cetearyl alcohol, glycerin, polysorbate 80, butylene glycol, ammonium acryloyldimethyltaurate/ VP copolymer, phenoxyethanol, salvia hispanica seed oil, calcium sodium borosilicate, cetearyl glucoside, tocopheryl acetate, chlorphenesin, malpighia emarginata (acerola) fruit extract, pentylene glycol, allantoin, carnosine, dipotassium glycyrrhizate, fragrance/parfum, dipropylene glycol, disodium EDTA, isononyl isononanoate, , tocopherol, glycine soja (soybean) oil, maltodextrin, citric acid, lecithin, centipeda cunninghamii extract, pentadecalactone, salvia hispanica seed extract, carrageenan, punica granatum fruit extract, zinc PCA, rubus fruticosus (blackberry) leaf extract, ceramide NP, sea salt, beta-sitosterol, sodium hyaluronate, oenothera biennis (evening primrose) oil, perilla ocymoides seed oil, helianthus annuus (sunflower) seed oil, BHT

Questions?

USA: 1-800-253-6500

* Please review the disclaimer below.