Aloe Vera Scent Anti Germ Spray
NDC Package 81670-002-14

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Aloe Vera Scent Anti Germ (alcohol) sprays is wet hands thoroughly with product and allow to dry without wiping. This formulation utilizes a spray delivery system. Marketed by F21 Opco,llc, this product is identified by NDC 81670-002 and is authorized under FDA application 505G(a)(3).

Identification & Billing

NDC Package Code
81670-002-14
Package Description
14 mL in 1 BOTTLE
Product Code
11-Digit Billing Format
81670000214
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Aloe Vera Scent Anti Germ
Non-Proprietary Name
Alcohol
Substance Name
Alcohol
Dosage Form
Spray - A liquid minutely divided as by a jet of air or steam.
Administration Route
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)
Usage Information
Wet hands thoroughly with product and allow to dry without wiping

Regulatory & Marketing

Labeler Name
F21 Opco,llc
Product Type
Human Otc Drug
FDA Application #
505G(a)(3)
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
10-22-2021
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 81670-002-14 identifies a specific commercial package of 14 ml in 1 bottle of Aloe Vera Scent Anti Germ, a human over the counter drug labeled by F21 Opco,llc. This spray is formulated for topical use and contains alcohol as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by F21 Opco,llc on October 22, 2021. The current certification is valid through December 31, 2026.

How is this F21 Opco,llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 81670000214. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
81670-002-14
11-Digit CMS (5-4-2)
81670-0002-14

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.