NDC Package 70116-025-01 Eezysun After Sun Cooling

Aniba Rossadora, Calendula Officinalis, Lavandula Officialls, Matricaria Chamomilla, - 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:
70116-025-01
Package Description:
1 TUBE in 1 CARTON / 100 mL in 1 TUBE
Product Code:
Proprietary Name:
Eezysun After Sun Cooling
Non-Proprietary Name:
Aniba Rossadora, Calendula Officinalis, Lavandula Officialls, Matricaria Chamomilla, Mentha Piperita, Sodium Hyaluronate
Substance Name:
Brazilian Rosewood Oil; Calendula Officinalis Flowering Top; Hyaluronate Sodium; Lavender Oil; Matricaria Chamomilla Whole; Peppermint Oil
Usage Information:
Shake well before useAdults: Apply up to three times per day as neededChildren: Use conservatively for children younger than two years
11-Digit NDC Billing Format:
70116002501
Product Type:
Human Otc Drug
Labeler Name:
Bio Earth Manufacturing (pty) Ltd
Dosage Form:
Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
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.
Sample Package:
No
Marketing Category:
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date:
05-23-2025
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 70116-025-01?

The NDC Packaged Code 70116-025-01 is assigned to a package of 1 tube in 1 carton / 100 ml in 1 tube of Eezysun After Sun Cooling, a human over the counter drug labeled by Bio Earth Manufacturing (pty) Ltd. The product's dosage form is cream and is administered via topical form.

Is NDC 70116-025 included in the NDC Directory?

Yes, Eezysun After Sun Cooling with product code 70116-025 is active and included in the NDC Directory. The product was first marketed by Bio Earth Manufacturing (pty) Ltd on May 23, 2025 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 70116-025-01?

The 11-digit format is 70116002501. 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
5-3-270116-025-015-4-270116-0025-01