NDC 10056-050 Artistry Skin Nutrition Renewing Reactivation Day Cream Spf 30

Avobenzone, Octisalate, Octocrylene

NDC Product Code 10056-050

NDC CODE: 10056-050

Proprietary Name: Artistry Skin Nutrition Renewing Reactivation Day Cream Spf 30 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
    • 10056-050 - Artistry Skin Nutrition Renewing Reactivation Day Cream Spf 30

NDC 10056-050-00

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

NDC Product Information

Artistry Skin Nutrition Renewing Reactivation Day Cream Spf 30 with NDC 10056-050 is a a human over the counter drug product labeled by Access Business Group Llc. The generic name of Artistry Skin Nutrition Renewing Reactivation Day Cream Spf 30 is avobenzone, octisalate, octocrylene. The product's dosage form is cream and is administered via topical form.

Dosage Form: Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.

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 Renewing Reactivation Day Cream Spf 30 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.


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)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
  • ISOHEXADECANE (UNII: 918X1OUF1E)
  • PENTYLENE GLYCOL (UNII: 50C1307PZG)
  • ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • PROPANEDIOL (UNII: 5965N8W85T)
  • BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
  • SHEA BUTTER (UNII: K49155WL9Y)
  • GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
  • PEG-100 STEARATE (UNII: YD01N1999R)
  • POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
  • CHIA SEED OIL (UNII: MC2LH51BO7)
  • POLYSORBATE 80 (UNII: 6OZP39ZG8H)
  • DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
  • AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • SPINACH (UNII: 6WO75C6WVB)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • CHLORPHENESIN (UNII: I670DAL4SZ)
  • ALLANTOIN (UNII: 344S277G0Z)
  • CARNOSINE (UNII: 8HO6PVN24W)
  • EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
  • OSMANTHUS FRAGRANS FLOWER (UNII: 4VA0BH57HU)
  • XANTHAN GUM (UNII: TTV12P4NEE)
  • TOCOPHEROL (UNII: R0ZB2556P8)
  • SOYBEAN OIL (UNII: 241ATL177A)
  • CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
  • GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
  • CHIA SEED (UNII: NU0OLX06F8)
  • LAURETH-12 (UNII: OAH19558U1)
  • POMEGRANATE (UNII: 56687D1Z4D)
  • CHLORELLA VULGARIS (UNII: RYQ4R60M02)
  • HYALURONATE SODIUM (UNII: YSE9PPT4TH)
  • POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
  • SODIUM BENZOATE (UNII: OJ245FE5EU)
  • TURMERIC (UNII: 856YO1Z64F)
  • CERAMIDE NP (UNII: 4370DF050B)
  • .BETA.-SITOSTEROL (UNII: S347WMO6M4)
  • 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: 09-22-2021 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 Renewing Reactivation Day Cream Spf 30 Product Label Images

Artistry Skin Nutrition Renewing Reactivation Day Cream Spf 30 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, glycerin, cetearyl alcohol, isohexadecane, pentylene glycol, isononyl isononanoate, butylene glycol, propanediol, butyloctyl salicylate, butyrospermum parkii (shea) butter, glyceryl stearate, PEG-100 stearate, ceteareth-20, salvia hispanica seed oil, polysorbate 80, polysilicone-11, ammonium acryloyldimethyltaurate/vp copolymer, phenoxyethanol, spinacia oleracea (spinach) leaf extract, tocopheryl acetate, chlorphenesin, fragrance/parfum, allantoin, carnosine, disodium EDTA, osmanthus fragrans flower extract, xanthan gum, tocopherol, glycine soja (soybean) oil, citric acid, dipotassium glycyrrhizate, lecithin, salvia hispanica seed extract, laureth-12, punica granatum fruit extract, chlorella vulgaris extract, sodium hyaluronate, potassium sorbate, sodium benzoate, curcuma longa (turmeric) root extract, ceramide NP, beta-sitosterol, 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.