0316-2036 NDC - BLUE LIZARD BABY SPF 50 SUNSCREEN ()

Drug Information

Product NDC: 0316-2036

Proprietary Name: Blue Lizard Baby SPF 50 Sunscreen

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Crown Laboratories
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:1/29/2020

Package Information

No. Package Code Package Description Billing Unit
10316-2036-105 mL in 1 PACKET (0316-2036-10)
20316-2036-3089 mL in 1 TUBE (0316-2036-30)
30316-2036-40148 mL in 1 BOTTLE, PLASTIC (0316-2036-40)
40316-2036-46148 mL in 1 TUBE (0316-2036-46)
50316-2036-50259 mL in 1 BOTTLE, PLASTIC (0316-2036-50)

NDC Record

Field Name Field Value Definition
PRODUCT NDC0316-2036The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEBlue Lizard Baby SPF 50 SunscreenThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE1/29/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMECrown LaboratoriesName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023