NDC 70306-5357 Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70306 - Giggle
- 70306-5357 - Sunscreen
Product Characteristics
Product Packages
NDC Code 70306-5357-4
Package Description: 118 mL in 1 TUBE
Product Details
What is NDC 70306-5357?
What are the uses for Sunscreen?
Which are Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Sunscreen 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:
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- ALCOHOL (UNII: 3K9958V90M)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- COCONUT ALKANES (UNII: 1E5KJY107T)
- ECHINACEA PURPUREA (UNII: QI7G114Y98)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- POLYGLYCERYL-2 SESQUIISOSTEARATE (UNII: LA272Q68GQ)
- POLYGLYCERYL-3 RICINOLEATE (UNII: MZQ63P0N0W)
- CRAMBE HISPANICA SUBSP. ABYSSINICA SEED OIL (UNII: 0QW9S92J3K)
- POLYGONUM AVICULARE TOP (UNII: ZCD6009IUF)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- SHEA BUTTER (UNII: K49155WL9Y)
- GINKGO (UNII: 19FUJ2C58T)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- WATER (UNII: 059QF0KO0R)
- ISOAMYL LAURATE (UNII: M1SLX00M3M)
- GLYCERIN (UNII: PDC6A3C0OX)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- BRASSICA RAPA SUBSP. OLEIFERA OIL (UNII: N4G8379626)
- COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
- MAGNESIUM SULFATE (UNII: DE08037SAB)
- SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
* 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".