NDC 55628-8477 Spf Rx - Anti-aging Sunscreen Spf 30

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:
55628-8477
Proprietary Name:
Spf Rx - Anti-aging Sunscreen Spf 30
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cal Pharma Llc
Labeler Code:
55628
Start Marketing Date: [9]
07-31-2017
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 55628-8477-4

Package Description: 120 g in 1 TUBE

Product Details

What is NDC 55628-8477?

The NDC code 55628-8477 is assigned by the FDA to the product Spf Rx - Anti-aging Sunscreen Spf 30 which is product labeled by Cal Pharma Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 55628-8477-4 120 g in 1 tube . 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 Spf Rx - Anti-aging Sunscreen Spf 30?

Apply liberally 15 minutes before sun exposure. Reapply:- After 80 minutes of swimming or sweating- At least every 2 hours. Immediately after towel drying.Sun Protection Measures: Spending time in the sun increases your risk of skin cancer & early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF of 15 or higher and other sun protection measures including:• limit time in the sun, especially from 10 a.m. - 2 p.m.• wear long-sleeve shirts, pants, hats, and sunglasses• Children under 6 months. Ask a doctor.

Which are Spf Rx - Anti-aging Sunscreen Spf 30 UNII Codes?

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

Which are Spf Rx - Anti-aging Sunscreen Spf 30 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:

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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".