NDC 75936-505 Super Power Sunscreen Mousse Spf 50 Supergoop

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:
75936-505
Proprietary Name:
Super Power Sunscreen Mousse Spf 50 Supergoop
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Taylor James, Ltd.
Labeler Code:
75936
Start Marketing Date: [9]
01-13-2017
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 75936-505-02

Package Description: 1 TUBE in 1 BOX / 100 mL in 1 TUBE (75936-505-01)

NDC Code 75936-505-04

Package Description: 1 TUBE in 1 BOX / 210 mL in 1 TUBE (75936-505-03)

NDC Code 75936-505-06

Package Description: 1 CAN in 1 BOX / 50 mL in 1 CAN (75936-505-05)

Product Details

What is NDC 75936-505?

The NDC code 75936-505 is assigned by the FDA to the product Super Power Sunscreen Mousse Spf 50 Supergoop which is product labeled by Taylor James, Ltd.. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 75936-505-02 1 tube in 1 box / 100 ml in 1 tube (75936-505-01), 75936-505-04 1 tube in 1 box / 210 ml in 1 tube (75936-505-03), 75936-505-06 1 can in 1 box / 50 ml in 1 can (75936-505-05). 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 Super Power Sunscreen Mousse Spf 50 Supergoop?

Stop use and ask a doctor if rash occurs

Which are Super Power Sunscreen Mousse Spf 50 Supergoop UNII Codes?

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

Which are Super Power Sunscreen Mousse Spf 50 Supergoop 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".