NDC 31645-152 Healthy Wear Pressed Bronzer Spf 50

NDC Product Code 31645-152

NDC 31645-152-02

Package Description: 1 CONTAINER in 1 BOX > 10.4 g in 1 CONTAINER (31645-152-01)

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

NDC Product Information

Healthy Wear Pressed Bronzer Spf 50 with NDC 31645-152 is a product labeled by Physicians Formula Inc. The generic name of Healthy Wear Pressed Bronzer Spf 50 is . The product's dosage form is and is administered via form.

Labeler Name: Physicians Formula Inc

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.

  • TALC (UNII: 7SEV7J4R1U)
  • MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
  • ASCORBYL PALMITATE (UNII: QN83US2B0N)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • GENISTEIN (UNII: DH2M523P0H)
  • ENOXOLONE (UNII: P540XA09DR)
  • ALPHA LIPOIC ACID (UNII: 73Y7P0K73Y)
  • TOMATO (UNII: Z4KHF2C175)
  • SQUALANE (UNII: GW89575KF9)
  • ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
  • .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
  • UBIDECARENONE (UNII: EJ27X76M46)
  • ZINC STEARATE (UNII: H92E6QA4FV)
  • EDETATE DISODIUM (UNII: 7FLD91C86K)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
  • SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
  • FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
  • FERRIC OXIDE RED (UNII: 1K09F3G675)
  • FERROSOFERRIC OXIDE (UNII: XM0M87F357)

Product Labeler Information

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

Labeler Name: Physicians Formula Inc
Labeler Code: 31645
Start Marketing Date: 03-01-2010 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.

Healthy Wear Pressed Bronzer Spf 50 Product Label Images

Healthy Wear Pressed Bronzer Spf 50 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

Active Ingredients:  Octinoxate 4%, Titanium Dioxide 21%, Zinc Oxide 3%Purpose: Sunscreen

Otc - Purpose

Uses . Helps prevent sunburn.  Higher SPF gives more sunburn protection . Retains SPF 50 after 40 minutes of activity in the water, sweating or perspiring

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.

Otc - When Using

  • When using this productKeep out of eyesRinse with water to remove

Otc - Ask Doctor

  • Stop use and ask a doctor ifRash or irritation develops and lasts

* Please review the disclaimer below.