NDC 53208-502 Isa Knox 365 Sun

NDC Product Code 53208-502

NDC 53208-502-02

Package Description: 1 CONTAINER in 1 BOX > 70 mL in 1 CONTAINER (53208-502-01)

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

NDC Product Information

Isa Knox 365 Sun with NDC 53208-502 is a product labeled by Lg Household And Healthcare, Inc.. The generic name of Isa Knox 365 Sun is . The product's dosage form is and is administered via form.

Labeler Name: Lg Household And Healthcare, Inc.

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)
  • ZINC OXIDE (UNII: SOI2LOH54Z)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
  • DIPROPYLENE GLYCOL (UNII: E107L85C40)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
  • SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
  • PANTHENOL (UNII: WV9CM0O67Z)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)
  • ETHYLPARABEN (UNII: 14255EXE39)
  • SACCHARIDE ISOMERATE (UNII: W8K377W98I)
  • ACETATE ION (UNII: 569DQM74SC)
  • DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)
  • ZINC STEARATE (UNII: H92E6QA4FV)
  • CETYL ETHYLHEXANOATE (UNII: 134647WMX4)
  • FRUIT (UNII: C2AIY4ERZC)
  • MARITIME PINE (UNII: 50JZ5Z98QY)

Product Labeler Information

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

Labeler Name: Lg Household And Healthcare, Inc.
Labeler Code: 53208
Start Marketing Date: 03-30-2010 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 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.

Isa Knox 365 Sun Product Label Images

Isa Knox 365 Sun 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

ZINC OXIDE 11.04%OCTINOXATE 7.02%TITANIUM DIOXIDE 4.03%

Warnings And Precautions

For external use only

Otc - Keep Out Of Reach Of Children

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

Otc - When Using

Keep out of eyes. Rinse with water to remove.

Otc - Stop Use

Stop use if a rash or irritation develops and lasts.

* Please review the disclaimer below.