NDC 62742-4041 Sun Tinted Solar Defense Organic Spf 30
NDC Product Code 62742-4041
Proprietary Name: Sun Tinted Solar Defense Organic Spf 30 What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name: What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
NDC Code Structure
- 62742 - Allure Labs, Inc.
- 62742-4041 - Sun Tinted Solar Defense Organic Spf 30
NDC 62742-4041-1
Package Description: 56.7 mL in 1 TUBE
NDC Product Information
Sun Tinted Solar Defense Organic Spf 30 with NDC 62742-4041 is a product labeled by Allure Labs, Inc.. The generic name of Sun Tinted Solar Defense Organic Spf 30 is . The product's dosage form is and is administered via form.
Labeler Name: Allure Labs, Inc.
Product Labeler Information
What is the Labeler Name?Name of Company corresponding to the labeler code segment of the Product NDC.
Labeler Name: Allure Labs, Inc.
Labeler Code: 62742
Start Marketing Date: 01-01-2010 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date: 12-31-2017 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.
Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. 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".
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Sun Tinted Solar Defense Organic Spf 30 Product Label Images
Sun Tinted Solar Defense Organic Spf 30 Product Labeling Information
The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.
Product Labeling Index
Otc - Purpose
Purpose:A physical organic UVA/UVB broad spectrum daily moisturizer. Provides an even skin tone and healthy glow. Ultimate protection against the aging effects of the sun and other environmental pollutants. Enriched with essential vitamins and anti-oxidants that prevent free facical damage. Preserves skin hydration for the entire day.Paraben FreeProvides Healthy even glowExcellent for sensitive skinChemical freeWater resistant
Indications & Usage
Directions:Apply liberally 15-30 minutes prior to sun exposure or as needed for a even skin tone. Reapply regulary or after prolonged swimming or activity.Indications:Sensitive skin, Sun exposure, uneven skin tone
Otc - Active Ingredient
Active Ingredients:Zinc Oxide 17%
Inactive Ingredient
Inactive Ingredients:Water (Aqua), Butylene Glycol, Glycerin, Caprylic/Capric Triglyceride, Glyceryl Stearate, PEG 100 Stearate, Sorbitan Stearate, Imperata Cylindrica Root Extract, Phenoxyethanol, Tocophery Linoleate, Ascorbyl Palmitate (Vitamin C), Lecithin, Tocopherol (Vitamin E), Xanthan Gum, Citric Acid, C13-14 Isoparaffin, PEG 8, Ethylhexylglycerin, Sodium Lactate, Micrococcus Lysate, Arabidopsis Extract, Plankton Extract, Teprenone, Phoenix dactylifera (date) Extract, Laureth-7, Disodium EDTA, Dipotassium Glycyrrizate, Caprylyl Glycol, Ascorbic Acid (Viamin C), Carbomer, Iron Oxides (CL 72124, Cl 7212 and Cl72123)
* Please review the disclaimer below.
