Vicks Vaposteam Liquid
NDC Package 69901-522-08

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Vicks Vaposteam (camphor (synthetic)) liquids is see important warnings under "When using this product"adults & children 2 years & over:add 1 tablespoon of solution to each quart of water or 1½ teaspoons of solution to each pint of wateradd solution directly to cold water only in a hot steam vaporizerfollow manufacturer's directions for using vaporizerbreathe in the medicated vaporsuse up to three times daily or as directed by a doctorchildren under 2 years: do not use. This formulation utilizes a liquid delivery system. Marketed by Kaz Usa, Inc, this product is identified by NDC 69901-522 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
69901-522-08
Package Description
1 BOTTLE, PLASTIC in 1 CARTON / 236 mL in 1 BOTTLE, PLASTIC
Product Code
69901-522
11-Digit Billing Format
69901052208
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Vicks Vaposteam
Non-Proprietary Name
Camphor (synthetic)
Substance Name
Camphor (synthetic)
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route
Respiratory (inhalation) - Administration within the respiratory tract by inhaling orally or nasally for local or systemic effect.
Active Ingredient(s)
CAMPHOR (SYNTHETIC) .062 g/mL
Usage Information
See important warnings under "When using this product"adults & children 2 years & over:add 1 tablespoon of solution to each quart of water or 1½ teaspoons of solution to each pint of wateradd solution directly to cold water only in a hot steam vaporizerfollow manufacturer's directions for using vaporizerbreathe in the medicated vaporsuse up to three times daily or as directed by a doctorchildren under 2 years: do not use

Regulatory & Marketing

Labeler Name
Kaz Usa, Inc
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
02-28-1995
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 69901-522-08 identifies a specific commercial package of 1 bottle, plastic in 1 carton / 236 ml in 1 bottle, plastic of Vicks Vaposteam, a human over the counter drug labeled by Kaz Usa, Inc. This liquid is formulated for respiratory (inhalation) use and contains camphor (synthetic) 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 Kaz Usa, Inc on February 28, 1995. The current certification is valid through December 31, 2026.

How is this Kaz Usa, Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 69901052208. 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)
69901-522-08
11-Digit CMS (5-4-2)
69901-0522-08

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