76309-550 NDC - SNUGZ SPF 50 BROAD SPECTRUM SUNSCREEN ()

Drug Information

Product NDC: 76309-550

Proprietary Name: SnugZ SPF 50 Broad Spectrum Sunscreen

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: SnugZ/USA, LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:1/1/2019

Package Information

No. Package Code Package Description Billing Unit
176309-550-0128 mL in 1 BOTTLE (76309-550-01)
276309-550-0256 mL in 1 BOTTLE (76309-550-02)
376309-550-04112 mL in 1 BOTTLE (76309-550-04)
476309-550-08226 mL in 1 BOTTLE (76309-550-08)
576309-550-1956 mL in 1 BOTTLE (76309-550-19)
676309-550-5130 mL in 1 TUBE (76309-550-51)
776309-550-6139.75 mL in 1 POUCH (76309-550-61)
876309-550-6285.17 mL in 1 POUCH (76309-550-62)

NDC Record

Field Name Field Value Definition
PRODUCT NDC76309-550The 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 NAMESnugZ SPF 50 Broad Spectrum 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 DATE1/1/2019This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMESnugZ/USA, LLCName 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