NDC Package 49643-818-30 Glycerol-saline Control

Glycerol-saline Diluent Injection Cutaneous; Intradermal; Subcutaneous - View Billable Units, 11-Digit Format, RxNorm

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:
49643-818-30
Package Description:
30 mL in 1 VIAL, MULTI-DOSE
Product Code:
Proprietary Name:
Glycerol-saline Control
Non-Proprietary Name:
Glycerol-saline Diluent
Substance Name:
Glycerin
Usage Information:
This product is used to relieve occasional constipation. Glycerin belongs to a class of drugs known as hyperosmotic laxatives. It works by drawing water into the intestines. This effect usually results in a bowel movement within 15 to 60 minutes. For adults, the normal frequency of bowel movements varies from once daily to 1 to 2 times weekly. For preschool-aged children, the normal frequency of bowel movements varies from once daily to once every other day. Constipation is best treated by drinking plenty of fluids, eating foods high in fiber, and exercising regularly.
11-Digit NDC Billing Format:
49643081830
NDC to RxNorm Crosswalk:
  • RxCUI: 1011991 - Trichothecium roseum allergenic extract 100 MG/mL Injectable Solution
  • RxCUI: 1011991 - Trichothecium roseum allergenic extract 100 MG/ML Injectable Solution
  • RxCUI: 1011991 - Trichothecium roseum extract 0.1 GM/ML Injectable Solution
  • RxCUI: 1011991 - Trichothecium roseum extract 100 MG/ML Injectable Solution
  • RxCUI: 1115265 - bluegum eucalyptus pollen extract 50 MG/ML Injectable Solution
Product Type:
Non-standardized Allergenic
Labeler Name:
Allermed Laboratories, Inc.
Dosage Form:
Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
Administration Route(s):
  • Cutaneous - Administration to the skin.
  • Intradermal - Administration within the dermis.
  • Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.
Active Ingredient(s):
Sample Package:
No
FDA Application Number:
BLA102211
Marketing Category:
BLA - A product marketed under an approved Biologic License Application.
Start Marketing Date:
03-12-1974
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.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
49643-818-055 mL in 1 VIAL, MULTI-DOSE
49643-818-1010 mL in 1 VIAL, MULTI-DOSE
49643-818-5050 mL in 1 VIAL, MULTI-DOSE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 49643-818-30?

The NDC Packaged Code 49643-818-30 is assigned to a package of 30 ml in 1 vial, multi-dose of Glycerol-saline Control, a non-standardized allergenic label labeled by Allermed Laboratories, Inc.. The product's dosage form is injection and is administered via cutaneous; intradermal; subcutaneous form.

Is NDC 49643-818 included in the NDC Directory?

Yes, Glycerol-saline Control with product code 49643-818 is active and included in the NDC Directory. The product was first marketed by Allermed Laboratories, Inc. on March 12, 1974 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 49643-818-30?

The 11-digit format is 49643081830. 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
5-3-249643-818-305-4-249643-0818-30