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  4. NDC Product Code: 62191-012 Oi Lin Sunmilk Sunscreen Spf 25

NDC 62191-012 Oi Lin Sunmilk Sunscreen Spf 25

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 62191-012?
  4. Oi Lin Sunmilk Sunscreen Spf 25 Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
62191-012
Proprietary Name:
Oi Lin Sunmilk Sunscreen Spf 25
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Sunrider Manufacturing L.p.
Labeler Code:
62191
Product Label ID:
1ac04cf8-1c30-42a7-b053-317af39f5d74
Start Marketing Date: [9]
04-23-2009
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 62191-012?

The NDC code 62191-012 is assigned by the FDA to the product Oi Lin Sunmilk Sunscreen Spf 25 which is product labeled by Sunrider Manufacturing L.p.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 62191-012-01 15 g in 1 tube , 62191-012-02 125 g in 1 bottle, plastic . 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 Oi Lin Sunmilk Sunscreen Spf 25?

RECOMMENDATION: APPPLY EVENLY TO ANY AREA OF THE BODY BEFORE SUN EXPOSURE TO PROVIDE MODERATE PROTECTION AGAINST SUNBURN.  REAPPLY AS NEEDED OR AFTER PROLONGED PHYSICAL ACTIVITY OR SWIMMING.  HIGHER SPF GIVES MORE SUNBURN PROTECTION.  RETAINS SPF AFTER 40 MINUTES OF ACTIVITY IN THE WATER.  CHILDREN UNDER 6 MONTHS OF AGE:CONSULT A DOCTOR BEFORE USE.

Which are Oi Lin Sunmilk Sunscreen Spf 25 UNII Codes?

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

Which are Oi Lin Sunmilk Sunscreen Spf 25 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".