NDC 11489-056 Botanics Daily Hand Therapy Sunscreen Spf 10
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 11489 - Bcm Ltd
- 11489-056 - Botanics Daily Hand Therapy Sunscreen Spf 10
Product Packages
NDC Code 11489-056-01
Package Description: 1 TUBE in 1 CARTON / 75 mL in 1 TUBE
Product Details
What is NDC 11489-056?
What are the uses for Botanics Daily Hand Therapy Sunscreen Spf 10?
Which are Botanics Daily Hand Therapy Sunscreen Spf 10 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are Botanics Daily Hand Therapy Sunscreen Spf 10 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)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- MINERAL OIL (UNII: T5L8T28FGP)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- PETROLATUM (UNII: 4T6H12BN9U)
- GLYCERIN (UNII: PDC6A3C0OX)
- SHEA BUTTER (UNII: K49155WL9Y)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- VACCINIUM MYRTILLUS LEAF (UNII: Y4U591OU70)
- CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- XANTHAN GUM (UNII: TTV12P4NEE)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
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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".