NDC 69435-1606-1 Mineralium Hdra Source Moisturizing Protector Spf 25

Package Information

The NDC Code 69435-1606-1 is assigned to a package of 50 ml in 1 container of Mineralium Hdra Source Moisturizing Protector Spf 25, labeled by Peer Pharm Ltd.. The product's dosage form is and is administered via form.

Field Name Field Value
NDC Code 69435-1606-1
Package Description 50 mL in 1 CONTAINER
Product Code 69435-1606
Proprietary Name 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.
Mineralium Hdra Source Moisturizing Protector Spf 25
11-Digit NDC Billing Format NDC Format for Billing
For insurance billing purposes the Centers for Medicare & Medicaid Services (CMS) created an 11 digit NDC derivative identifier. If the NDC Package code is less than 11 digits the code must be padded with leading zeros. The leading zeros must be added to the appropriate segment to create a 5-4-2 configuration.
Labeler Name Peer Pharm Ltd.
Sample Package Sample Package?
This field Indicates whether this package is a sample packaging or not.
Start Marketing Date 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 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 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".
NDC Code Structure
This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

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