NDC 58418-425 Fresh Skin Organics
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Product Packages
NDC Code 58418-425-00
Package Description: 15 mL in 1 PACKET
NDC Code 58418-425-01
Package Description: 30 mL in 1 BOTTLE, DISPENSING
NDC Code 58418-425-02
Package Description: 60 mL in 1 BOTTLE, DISPENSING
NDC Code 58418-425-04
Package Description: 120 mL in 1 BOTTLE, DISPENSING
NDC Code 58418-425-05
Package Description: 15 mL in 1 BOTTLE, DISPENSING
NDC Code 58418-425-08
Package Description: 240 mL in 1 BOTTLE, DISPENSING
NDC Code 58418-425-09
Package Description: 240 mL in 1 BOTTLE, PUMP
NDC Code 58418-425-12
Package Description: 360 mL in 1 BOTTLE, PUMP
NDC Code 58418-425-16
Package Description: 480 mL in 1 BOTTLE, PUMP
NDC Code 58418-425-28
Package Description: 3840 mL in 1 BOTTLE, PUMP
NDC Code 58418-425-34
Package Description: 100.55 mL in 1 TUBE
NDC Code 58418-425-55
Package Description: 211200 mL in 1 DRUM
NDC Code 58418-425-64
Package Description: 1920 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 58418-425?
What are the uses for Fresh Skin Organics?
Which are Fresh Skin Organics UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Fresh Skin Organics 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:
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- PROPANEDIOL (UNII: 5965N8W85T)
- CASTOR OIL (UNII: D5340Y2I9G)
- ROSEMARY OIL (UNII: 8LGU7VM393)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- KUKUI NUT OIL (UNII: TP11QR7B8R)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
- GLYCERIN (UNII: PDC6A3C0OX)
- SHEA BUTTER (UNII: K49155WL9Y)
- JOJOBA OIL (UNII: 724GKU717M)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- LAURIC ACID (UNII: 1160N9NU9U)
- CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE (UNII: FJ1H6M2JG9)
- AVOCADO OIL (UNII: 6VNO72PFC1)
- XANTHAN GUM (UNII: TTV12P4NEE)
- PEG-30 DIPOLYHYDROXYSTEARATE (UNII: 9713Q0S7FO)
- ROSA CANINA FRUIT OIL (UNII: CR7307M3QZ)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
- CAPRYLIC ACID (UNII: OBL58JN025)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- CAMELLIA SINENSIS WHOLE (UNII: C5M4585ZBZ)
- ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
- RASPBERRY SEED OIL (UNII: 9S8867952A)
- SQUALANE (UNII: GW89575KF9)
* 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".