NDC 65435-0116 Safe Sea Sunscreen With Jellyfish Sting Protective Spf 15

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:
65435-0116
Proprietary Name:
Safe Sea Sunscreen With Jellyfish Sting Protective Spf 15
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Nidaria Technology Ltd.
Labeler Code:
65435
Start Marketing Date: [9]
11-12-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 65435-0116-5

Package Description: 118 mL in 1 BOTTLE

Product Details

What is NDC 65435-0116?

The NDC code 65435-0116 is assigned by the FDA to the product Safe Sea Sunscreen With Jellyfish Sting Protective Spf 15 which is product labeled by Nidaria Technology Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 65435-0116-5 118 ml in 1 bottle . 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 Safe Sea Sunscreen With Jellyfish Sting Protective Spf 15?

- Adults and children six months of age and older. Apply Liberally to all exposed areas 10 minutes before sun or water exposure.  - Ensure complete coverage.  - Reapply after prolonged swimmimg and towel drying.

Which are Safe Sea Sunscreen With Jellyfish Sting Protective Spf 15 UNII Codes?

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

Which are Safe Sea Sunscreen With Jellyfish Sting Protective Spf 15 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".