NDC 71014-021 Foundation Sunscreen Face Stick Broad Spectrum Spf 35 Cooly Beige
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71014 - Eai-jr286, Inc.
- 71014-021 - Foundation Sunscreen Face Stick Broad Spectrum Spf 35 Cooly Beige
Product Packages
NDC Code 71014-021-02
Package Description: 1 CYLINDER in 1 BOX / 11 g in 1 CYLINDER (71014-021-01)
Product Details
What is NDC 71014-021?
What are the uses for Foundation Sunscreen Face Stick Broad Spectrum Spf 35 Cooly Beige?
Which are Foundation Sunscreen Face Stick Broad Spectrum Spf 35 Cooly Beige UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Foundation Sunscreen Face Stick Broad Spectrum Spf 35 Cooly Beige 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:
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- HEXYLDECYL ISOSTEARATE (UNII: 3V20TC06U5)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- MICA (UNII: V8A1AW0880)
- CERESIN (UNII: Q1LS2UJO3A)
- PARAFFIN (UNII: I9O0E3H2ZE)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- SYNTHETIC WAX (1200 MW) (UNII: Q3Z4BCH099)
- TOCOPHEROL (UNII: R0ZB2556P8)
- STEARYL GLYCYRRHETINATE (UNII: 3YYE6VJS0P)
* Please review the disclaimer below.
[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".