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  5. NDC Package Code: 37808-397-34 Vaproizing

NDC Package 37808-397-34 Vaproizing

Camphor Liquid Respiratory (inhalation) - 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:
37808-397-34
Package Description:
1 BOTTLE, PLASTIC in 1 CARTON / 237 mL in 1 BOTTLE, PLASTIC
Product Code:
37808-397
Proprietary Name:
Vaproizing
Non-Proprietary Name:
Camphor
Substance Name:
Camphor (natural)
Usage Information:
See important warnings under "When using this produc"adults & children 2 years of age and older: use 1 tablespoon of solution for each quart of water or 1 1/2 teaspoons of solution for each pint of wateradd solution directlty to cold water only in a hot steam vaporizerfollow manufacture's directins for using vaporizerbreathe in medicated vaporsmay be repeated up to 3 times a daychildren under 2 years: ask a doctor
11-Digit NDC Billing Format:
37808039734
NDC to RxNorm Crosswalk:
Product Type:
Human Otc Drug
Labeler Name:
H E B
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(s):
Respiratory (inhalation) - Administration within the respiratory tract by inhaling orally or nasally for local or systemic effect.
Active Ingredient(s):
CAMPHOR (NATURAL) 62 mg/mL
Sample Package:
No
FDA Application Number:
M012
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
10-06-2010
Listing Expiration Date:
12-31-2026
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 37808-397-34?

The NDC Packaged Code 37808-397-34 is assigned to a package of 1 bottle, plastic in 1 carton / 237 ml in 1 bottle, plastic of Vaproizing, a human over the counter drug labeled by H E B. The product's dosage form is liquid and is administered via respiratory (inhalation) form.

Is NDC 37808-397 included in the NDC Directory?

Yes, Vaproizing with product code 37808-397 is active and included in the NDC Directory. The product was first marketed by H E B on October 06, 2010 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 37808-397-34?

The 11-digit format is 37808039734. 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
5-3-237808-397-345-4-237808-0397-34