NDC 40061-990 Patricks Sunscreen

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
40061-990
Proprietary Name:
Patricks Sunscreen
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
O.p. Products, Inc.
Labeler Code:
40061
Start Marketing Date: [9]
04-28-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Product Packages

NDC Code 40061-990-08

Package Description: 8 PACKET in 1 CELLO PACK / 8.75 g in 1 PACKET (40061-990-10)

NDC Code 40061-990-11

Package Description: 8.75 g in 1 PACKET

NDC Code 40061-990-50

Package Description: 50 PACKET in 1 BOX / 8.75 g in 1 PACKET (40061-990-10)

Product Details

What is NDC 40061-990?

The NDC code 40061-990 is assigned by the FDA to the product Patricks Sunscreen which is product labeled by O.p. Products, Inc.. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 40061-990-08 8 packet in 1 cello pack / 8.75 g in 1 packet (40061-990-10), 40061-990-11 8.75 g in 1 packet , 40061-990-50 50 packet in 1 box / 8.75 g in 1 packet (40061-990-10). This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Patricks Sunscreen?

Apply liberally 30 minutes before sun exposure Children under 6 months of age consult a doctor Reapply as needed or after towel drying, swimming or sweating

Which are Patricks Sunscreen UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Patricks Sunscreen Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".