NDC 11822-1235 Ultimate Sheer Sunscreen Spf 70 Daylogic

NDC Product Code 11822-1235

NDC CODE: 11822-1235

Proprietary Name: Ultimate Sheer Sunscreen Spf 70 Daylogic 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

  • 11822 - Rite Aid

NDC 11822-1235-2

Package Description: 43 g in 1 PACKAGE

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

NDC Product Information

Ultimate Sheer Sunscreen Spf 70 Daylogic with NDC 11822-1235 is a product labeled by Rite Aid. 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.

  • YELLOW WAX (UNII: 2ZA36H0S2V)
  • BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
  • ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
  • CAPRYLYL GLYCOL (UNII: 00YIU5438U)
  • NEOPENTYL GLYCOL DIETHYLHEXANOATE (UNII: U68ZV6W62C)
  • NEOPENTYL GLYCOL DIISOSTEARATE (UNII: 4M6OQ34JWW)
  • OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
  • CERESIN (UNII: Q1LS2UJO3A)
  • PARAFFIN (UNII: I9O0E3H2ZE)
  • PETROLATUM (UNII: 4T6H12BN9U)
  • POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) (UNII: T9296U138P)
  • HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)

Product Labeler Information

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

Labeler Name: Rite Aid
Labeler Code: 11822
Start Marketing Date: 12-22-2016 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: 12-31-2019 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.

Ultimate Sheer Sunscreen Spf 70 Daylogic Product Label Images