NDC 70604-030 Silkshield All Mineral Sunscreen With Trihex Technology

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
70604-030
Proprietary Name:
Silkshield All Mineral Sunscreen With Trihex Technology
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
70604
Start Marketing Date: [9]
09-17-2021
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Code Structure Chart

Product Details

What is NDC 70604-030?

The NDC code 70604-030 is assigned by the FDA to the product Silkshield All Mineral Sunscreen With Trihex Technology which is product labeled by Alastin Skincare, Inc.. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 70604-030-00 12 tube in 1 carton / 5 g in 1 tube, 70604-030-02 1 tube in 1 carton / 53.8 g in 1 tube, 70604-030-04 113 g in 1 tube , 70604-030-99 12 g in 1 tube . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Silkshield All Mineral Sunscreen With Trihex Technology?

Apply liberally 15 minutes before sun exposureReapply:After 40 minutes of swimming or sweatingImmediately after towel dryingAt least every two hoursChildren under 6 months of age:Ask a doctor.Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:Limit time in the sun, especially from 10am - 2pmWear long-sleeved shirts, pants, hats and sunglasses

Which are Silkshield All Mineral Sunscreen With Trihex Technology UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Silkshield All Mineral Sunscreen With Trihex Technology Inactive Ingredients UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
  • DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
  • SQUALANE (UNII: GW89575KF9)
  • POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE (4000 MPA.S) (UNII: RLA2U05Z4Q)
  • HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
  • METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q)
  • TRIETHOXYSILYLETHYL POLYDIMETHYLSILOXYETHYL HEXYL DIMETHICONE (UNII: X75PL53TZJ)
  • PALMITOYL HEXAPEPTIDE-12 (UNII: HO4ZT5S86C)
  • PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M)
  • DUNALIELLA SALINA (UNII: F4O1DKI9A6)
  • ECTOINE (UNII: 7GXZ3858RY)
  • 1-(4-HYDROXY-3-METHOXYPHENYL)-DECAN-3-ONE (UNII: BO24ID7E9U)
  • TOCOPHEROL (UNII: R0ZB2556P8)
  • MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
  • STEARALKONIUM HECTORITE (UNII: OLX698AH5P)
  • DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
  • PENTAERYTHRITYL TETRAISOSTEARATE (UNII: 9D7IK5483F)
  • PROPYLENE CARBONATE (UNII: 8D08K3S51E)

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Product Footnotes

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

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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.

[12] 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".