NDC 75885-030 Putto Secret Uv Face

NDC Product Code 75885-030

NDC CODE: 75885-030

Proprietary Name: Putto Secret Uv Face 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.

NDC Code Structure

  • 75885 - Agabang & Company

NDC 75885-030-01

Package Description: 80 mL in 1 TUBE

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Putto Secret Uv Face with NDC 75885-030 is a product labeled by Agabang & Company. The product's dosage form is and is administered via form.

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.

  • CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
  • GLECHOMA HEDERACEA FLOWERING TOP (UNII: 2458J91U39)
  • HOUTTUYNIA CORDATA FLOWERING TOP (UNII: RH041UUZ22)
  • PLANTAGO ASIATICA (UNII: 5F5728J5E8)
  • SQUALENE (UNII: 7QWM220FJH)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • DIPROPYLENE GLYCOL (UNII: E107L85C40)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • MORUS ALBA LEAF (UNII: M8YIA49Q2P)
  • ULMUS DAVIDIANA ROOT (UNII: URQ79U8261)
  • ALGELDRATE (UNII: 03J11K103C)
  • PANTHENOL (UNII: WV9CM0O67Z)

Product Labeler Information

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

Labeler Name: Agabang & Company
Labeler Code: 75885
Start Marketing Date: 08-26-2013 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: 12-31-2017 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: I - INACTIVATED, the listing data was inactivated by the FDA. 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.

Putto Secret Uv Face Product Label Images

Putto Secret Uv Face 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

Otc - Active Ingredient

Titanium dioxide

Inactive Ingredient

Houttuynia cordata ext, glechoma hederacea flower/leaf/stem ext, plantago asiatica ext, cyclopentasiloxane, butylene glycol, crprylic/capric triglyceride, dipropylene glycol, zinc oxide, morus alba leaf ext, ulmus davidiana root ext, cyclomethicone, squalane, peg-10 dimethicone, cetyl peg/ppg-10/1 dimethicone, sodium chloride, dimethicone/vinyl dimethicone crosspolymer, dimethicone, stearalkonium hectorite, propylene carbonate, aluminum hydroxide, aluminum stearate, caprylhydroxamic acid, caprylyl glycol, glycerin, 1,2-hexanediol, tocopheryl acetate, betaine, panthenol, ceramide 3, distearyldimonium chloride, sodium hyaluronate, beta glucan, bentonite, fragrance

Otc - Purpose

Sun screen

Otc - Keep Out Of Reach Of Children

Keep out of reach of the children

Indications & Usage

Gently spread a fair amount over face, neck, arm and etc esposed to UV rays

Warnings

Do not apply to sensitive skinstore in a cool, dry place

Dosage & Administration

For external use only

* Please review the disclaimer below.