NDC 70342-102 Sun Bathe Sunscreen Spf 20
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 70342-102?
What are the uses for Sun Bathe Sunscreen Spf 20?
Which are Sun Bathe Sunscreen Spf 20 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Sun Bathe Sunscreen Spf 20 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:
- WATER (UNII: 059QF0KO0R)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM STEARATE (UNII: QU7E2XA9TG)
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- SORBITOL (UNII: 506T60A25R)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM MYRISTATE (UNII: 06BLC4V0IV)
- SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)
- CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)
- TROLAMINE (UNII: 9O3K93S3TK)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- POLYQUATERNIUM-16 (N-VINYLPYRROLIDINONE:3-METHYL-1-VINYLIMIDAZOLIUM CHLORIDE (5:5)) (UNII: 1KX12A42IJ)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- EDETATE SODIUM (UNII: MP1J8420LU)
- PENTASODIUM PENTETATE (UNII: 961TOZ5L7T)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- POLYAMIDE-3 (30000 MW) (UNII: 9AO559AXEB)
- SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)
- POLYETHYLENE GLYCOL 800 (UNII: UH6KR4953D)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- PROPYLENE GLYCOL-HYDROXYETHYLCELLULOSE STEARYLDIMONIUM CHLORIDE (UNII: 3479326GXB)
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[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".