NDC 11822-1235 Ultimate Sheer Sunscreen Spf 70 Daylogic
NDC Product 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.
Non-Proprietary Name: What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
NDC Code Structure
- 11822 - Rite Aid
- 11822-1235 - Ultimate Sheer Sunscreen Spf 70
NDC 11822-1235-2
Package Description: 43 g in 1 PACKAGE
NDC Product Information
Ultimate Sheer Sunscreen Spf 70 Daylogic with NDC 11822-1235 is a product labeled by Rite Aid. The generic name of Ultimate Sheer Sunscreen Spf 70 Daylogic is . The product's dosage form is and is administered via form.
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.
- 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 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’.
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