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  5. NDC Package Code: 83021-877-07 Anubis Barcelona

NDC Package 83021-877-07 Anubis Barcelona

Glycerin,Sorbitol,Aloe Barbadensis Leaf Juice Concentrate Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
83021-877-07
Package Description:
1.5 mL in 1 VIAL, SINGLE-USE
Product Code:
83021-877
Proprietary Name:
Anubis Barcelona
Non-Proprietary Name:
Glycerin, Sorbitol, Aloe Barbadensis Leaf Juice
Substance Name:
1,2-hexanediol; Aloe Vera Leaf; Ethylhexylglycerin; Fd&c Blue No. 1; Glycerin; Hyaluronate Sodium; Leuconostoc/radish Root Ferment Filtrate; Phenoxyethanol; Saccharomyces Lysate; Sorbitol; Water
11-Digit NDC Billing Format:
83021087707
Product Type:
Human Otc Drug
Labeler Name:
Anubis Cosmetics Sl
Dosage Form:
Concentrate - A liquid preparation of increased strength and reduced volume which is usually diluted prior to administration.
Administration Route(s):
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
    • Active Ingredient(s):
  • 1,2-HEXANEDIOL .0165 g/1.5mL
  • ALOE VERA LEAF .008955 g/1.5mL
  • ETHYLHEXYLGLYCERIN .0015 g/1.5mL
  • FD&C BLUE NO. 1 .000009 g/1.5mL
  • GLYCERIN .16875 g/1.5mL
  • HYALURONATE SODIUM .0075 g/1.5mL
  • LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE .000015 g/1.5mL
  • PHENOXYETHANOL .0141 g/1.5mL
  • SACCHAROMYCES LYSATE .00075 g/1.5mL
  • SORBITOL .0525 g/1.5mL
  • WATER 1.219341 mL/1.5mL
    • Pharmacologic Class(es):
  • Allergens - [CS]
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Glycerol - [CS]
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Increased IgG Production - [PE] (Physiologic Effect)
  • Non-Standardized Chemical Allergen - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    M016
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    10-19-2022
    End Marketing Date:
    01-14-2027
    Exclude Flag:
    N
    Code Structure:

    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.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 83021-877-07?

    The NDC Packaged Code 83021-877-07 is assigned to a package of 1.5 ml in 1 vial, single-use of Anubis Barcelona, a human over the counter drug labeled by Anubis Cosmetics Sl. The product's dosage form is concentrate and is administered via topical form.

    Is NDC 83021-877 included in the NDC Directory?

    Yes, Anubis Barcelona with product code 83021-877 is active and included in the NDC Directory. The product was first marketed by Anubis Cosmetics Sl on October 19, 2022.

    What is the 11-digit format for NDC 83021-877-07?

    The 11-digit format is 83021087707. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-283021-877-075-4-283021-0877-07