NDC 14783-971 Brightening And Moisturizing Facial Spf 30

NDC Product Code 14783-971

NDC 14783-971-02

Package Description: 1 BOTTLE in 1 BOX > 30 mL in 1 BOTTLE (14783-971-01)

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

NDC Product Information

Brightening And Moisturizing Facial Spf 30 with NDC 14783-971 is a product labeled by Ventura International Ltd. The generic name of Brightening And Moisturizing Facial Spf 30 is . The product's dosage form is and is administered via form.

Labeler Name: Ventura International Ltd

Dosage Form: -

Product Type: 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)
  • DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
  • CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
  • PHENETHYL BENZOATE (UNII: 0C143929GK)
  • TROLAMINE (UNII: 9O3K93S3TK)
  • CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
  • TRIETHYLHEXANOIN (UNII: 7K3W1BIU6K)
  • POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • STEARYL DIMETHICONE (400 MPA.S AT 50C) (UNII: R327X197HY)
  • POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
  • XANTHAN GUM (UNII: TTV12P4NEE)
  • CETYL ALCOHOL (UNII: 936JST6JCN)
  • GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
  • CHLORPHENESIN (UNII: I670DAL4SZ)
  • MOTH BEAN (UNII: H7938ON8E5)
  • DIMETHYLMETHOXY CHROMANYL PALMITATE (UNII: 5G222ZDK7U)
  • PEG-75 STEARATE (UNII: OT38R0N74H)
  • SODIUM COCOYL GLUTAMATE (UNII: BMT4RCZ3HG)
  • EDETATE SODIUM (UNII: MP1J8420LU)
  • CETETH-20 (UNII: I835H2IHHX)
  • STEARETH-20 (UNII: L0Q8IK9E08)
  • BUTYLPARABEN (UNII: 3QPI1U3FV8)
  • SORBIC ACID (UNII: X045WJ989B)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
  • HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)
  • LIMONENE, (+)- (UNII: GFD7C86Q1W)
  • LINALOOL, (+/-)- (UNII: D81QY6I88E)
  • BENZYL SALICYLATE (UNII: WAO5MNK9TU)
  • .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)

Product Labeler Information

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

Labeler Name: Ventura International Ltd
Labeler Code: 14783
Start Marketing Date: 09-26-2016 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 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Brightening And Moisturizing Facial Spf 30 Product Label Images

Brightening And Moisturizing Facial 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

Other

Drug Facts

  • Skin Cancer / Skin Aging Alert: Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to help prevent sunburn, not skin cancer or early skin aging.For external use only.

Dist. by Ventura Int Ltd. DBA BelcorpUSA, Miami, FL 33126

Otc - Purpose

Active IngredientsPurposeAVOBENZONE 3.00%SunscreenENSULIZOLE 3.00 %SunscreenOCTISALATE 5.00 %SunscreenOCTOCRYLENE 5.00 %SunscreenOXYBENZONE 6.00 %Sunscreen

Uses

  • Helps prevent sunburn.

Otc - Do Not Use

  • Do not use on damaged or broken skin.

Otc - When Using

  • When using this product keep out of eyes. Rinse with water to remove.

Otc - Stop Use

  • Stop use and ask a doctor if rash occurs.

Otc - Keep Out Of Reach Of Children

  • Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Apply liberally and evenly 15 minutes before sun exposure.Reapply at least every 2 hoursUse a water resistant sunscreen if swimming or sweating.Children under 6 months of age: Ask a doctor

Other Information

  • Protect the product in this container from excessive heat and direct sun.

Inactive Ingredients

WATER, DICAPRYLYL CARBONATE, CETEARYL ALCOHOL, PHENETHYL BENZOATE, TRIETHANOLAMINE, CYCLOPENTASILOXANE, PROPYLENE GLYCOL, METHYL METHACRYLATE CROSSPOLYMER, SORBITAN STEARATE, TRIETHYLHEXANOIN, POTASSIUM CETYL PHOSPHATE, PHENOXYETHANOL, DIMETHICONE, STEARYL DIMETHICONE, CETEARETH-20, XANTHAN GUM, CETYL ALCOHOL, GLYCERYL STEARATE, CHLORPHENESIN, FRAGRANCE, VIGNA ACONITIFOLIA SEED EXTRACT, DIMETHYLMETHOXY CHROMANYL PALMITATE, PEG-75 STEARATE, SODIUM COCOYL GLUTAMATE, TETRASODIUM EDTA, CETETH-20, STEARETH-20, BUTYLPARABEN, SORBIC ACID, METHYLPARABEN, ALPHA-ISOMETHYL IONONE, HYDROXYCITRONELLAL, d-LIMONENE, LINALOOL, BENZYL SALICYLATE, CITRONELLOL.

* Please review the disclaimer below.