71175-0004 NDC - ZAOL DOCTORS ORDER SYNERGY BOOSTER (PANTHENOL, SALICYLIC ACID, MENTHOL)

Drug Information

Product NDC: 71175-0004

Proprietary Name: ZAOL DOCTORS ORDER SYNERGY BOOSTER

Non Proprietary Name: Panthenol, Salicylic Acid, Menthol

Active Ingredient(s):
  • .25 g/100mL SALICYLIC ACID;
  • .2 g/100mL PANTHENOL;
  • .3 g/100mL MENTHOL


Administration Route(s): TOPICAL

Dosage Form(s): LIQUID

Labeler Information

Labeler Name: zaol
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date:1/10/2017

Package Information

No. Package Code Package Description Billing Unit
171175-0004-1100 mL in 1 BOTTLE, WITH APPLICATOR (71175-0004-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC71175-0004The 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 NAMEZAOL DOCTORS ORDER SYNERGY BOOSTERThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEPanthenol, Salicylic Acid, MentholThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe translation of the dosage form Code submitted by the firm.
ROUTE NAMETOPICALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE1/10/2017This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED DRUG OTHERProduct 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.
LABELER NAMEzaolName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMESALICYLIC ACID; PANTHENOL; MENTHOLThis is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH.25; .2; .3 
ACTIVE INGRED UNITg/100mL; g/100mL; g/100mL 

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This page was last updated on: 7/15/2019