NDC 73690-027 Versed Guards Up Daily Mineral Sunscreen Broad Spectrum Spf 35

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:
73690-027
Proprietary Name:
Versed Guards Up Daily Mineral Sunscreen Broad Spectrum Spf 35
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
73690
Start Marketing Date: [9]
10-01-2021
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 73690-027?

The NDC code 73690-027 is assigned by the FDA to the product Versed Guards Up Daily Mineral Sunscreen Broad Spectrum Spf 35 which is product labeled by Offspring Beauty Co.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 73690-027-01 50 ml in 1 tube , 73690-027-02 75 ml 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 Versed Guards Up Daily Mineral Sunscreen Broad Spectrum Spf 35?

Apply liberally and evenly 15 minutes before sun exposureReapply at least every 2 hoursUse a water resistant sunscreen if swimming or sweating, immediately after toweling drying, and at least every 2 hoursChildren under 6 months of age: ask a doctorSun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and othe sun protection measures including: limit time in sun, especially from 10 a.m. to 2 p.m. and wear long-sleeved shirts, pants, hats, and sunglasses

Which are Versed Guards Up Daily Mineral Sunscreen Broad Spectrum Spf 35 UNII Codes?

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

Which are Versed Guards Up Daily Mineral Sunscreen Broad Spectrum Spf 35 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".