NDC 71055-100 Ice Sun Bc Air Puff

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:
71055-100
Proprietary Name:
Ice Sun Bc Air Puff
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
71055
Start Marketing Date: [9]
10-21-2016
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 71055-100?

The NDC code 71055-100 is assigned by the FDA to the product Ice Sun Bc Air Puff which is product labeled by Popco Co.,ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71055-100-02 1 bottle in 1 package / 100 ml in 1 bottle (71055-100-01). 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 Ice Sun Bc Air Puff?

• Turn bottle lid to “ON” state. Shake the bottle well, pump it 4-5 times and take out the puff and apply it on skin.• Apply liberally 15 minutes before sun exposure.• Reapply at least every 2 hours.• Use a water-resistant sunscreen if swimming or sweating.• Sun 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 other sun protection measures including: Limit time in the sun, especially from 10 a.m. - 2 p.m. Wear long-sleeved shirts, pants, hats, and sunglasses.• Children under 6 months of age: ask a doctor

Which are Ice Sun Bc Air Puff UNII Codes?

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

Which are Ice Sun Bc Air Puff 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".