NDC Package 70157-027-03 Standard Procedure Spf 50 Sunscreen Face And Body

Avobenzone,Homosalate,Octisalate,Octocrylene Lotion Topical - View Billable Units, 11-Digit Format, RxNorm

Package Information
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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:

70157-027-03

Package Description:

250 mL in 1 BOTTLE, PLASTIC

Product Code:

70157-027

Proprietary Name:

Standard Procedure Spf 50 Sunscreen Face And Body

Non-Proprietary Name:

Avobenzone, Homosalate, Octisalate, Octocrylene

Substance Name:

Avobenzone; Homosalate; Octisalate; Octocrylene

Usage Information:

Stop use and ask a doctor if rash occurs

11-Digit NDC Billing Format:

70157002703

Product Type:

Human Otc Drug

Labeler Name:

Baxter Laboratories

Dosage Form:

Lotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2

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.

Active Ingredient(s):

Sample Package:

FDA Application Number:

M020

Marketing Category:

OTC MONOGRAPH DRUG -

Start Marketing Date:

05-30-2025

Listing Expiration Date:

12-31-2026

Exclude Flag:

Code Structure:

70157 - Baxter Laboratories
- 70157-027 - Standard Procedure Spf 50 Sunscreen Face And Body
  - 70157-027-03 - 250 mL in 1 BOTTLE, PLASTIC

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 Code	Package Description
70157-027-01	60 mL in 1 BOTTLE, PLASTIC
70157-027-02	100 mL in 1 BOTTLE, PLASTIC
70157-027-04	500 mL in 1 BOTTLE, PUMP

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 70157-027-03?

The NDC Packaged Code 70157-027-03 is assigned to a package of 250 ml in 1 bottle, plastic of Standard Procedure Spf 50 Sunscreen Face And Body, a human over the counter drug labeled by Baxter Laboratories. The product's dosage form is lotion and is administered via topical form.

Is NDC 70157-027 included in the NDC Directory?

Yes, Standard Procedure Spf 50 Sunscreen Face And Body with product code 70157-027 is active and included in the NDC Directory. The product was first marketed by Baxter Laboratories on May 30, 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 70157-027-03?

The 11-digit format is 70157002703. 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 Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-3-2	70157-027-03	5-4-2	70157-0027-03

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