10157-9905 NDC - BLISTEX ADVANCED CARE (BLISTEX MEDICATED BALM, BLISTEX COMPLETE MOISTURE, BLISTEX FIVE STAR LIP BALM - BROAD SPECTRUM, BLISTEX SUPERFRUIT SOOTHER) (DIMETHICONE, OCTINOXATE, OCTISALATE, AVOBENZONE, AND HOMOSALATE)

Drug Information

Product NDC: 10157-9905

Proprietary Name: Blistex Advanced Care (Blistex Medicated Balm, Blistex Complete Moisture, Blistex Five Star Lip Balm - Broad Spectrum, Blistex Superfruit Soother)

Non Proprietary Name: Dimethicone, Octinoxate, Octisalate, Avobenzone, and Homosalate

Active Ingredient(s):


Administration Route(s):

Dosage Form(s): KIT

Labeler Information

Labeler Name: Blistex Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part347
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date:8/26/2019

Package Information

No. Package Code Package Description Billing Unit
110157-9905-11 KIT in 1 CARTON (10157-9905-1) * 4.25 g in 1 CYLINDER * 4.25 g in 1 CYLINDER * 4.25 g in 1 CYLINDER * 4.25 g in 1 CYLINDER

NDC Record

Field Name Field Value Definition
PRODUCT NDC10157-9905The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates 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.
PROPRIETARY NAMEBlistex Advanced Care (Blistex Medicated Balm, Blistex Complete Moisture, Blistex Five Star Lip Balm - Broad Spectrum, Blistex Superfruit Soother)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 NAMEDimethicone, Octinoxate, Octisalate, Avobenzone, and HomosalateThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEKITThe translation of the dosage form Code submitted by the firm.
START MARKETING DATE8/26/2019This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH FINALProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
APPLICATION NUMBERpart347This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
LABELER NAMEBlistex IncName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023