NDC 69417-100 Indigo Soothing Triple Recovery Cream
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 69417-100?
What are the uses for Indigo Soothing Triple Recovery Cream?
Which are Indigo Soothing Triple Recovery Cream UNII Codes?
The UNII codes for the active ingredients in this product are:
- OATMEAL (UNII: 8PI54V663Y)
- OATMEAL (UNII: 8PI54V663Y) (Active Moiety)
Which are Indigo Soothing Triple Recovery Cream 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)
- SQUALANE (UNII: GW89575KF9)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPANEDIOL (UNII: 5965N8W85T)
- DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
- DIISOSTEARYL MALATE (UNII: QBS8A3XZGQ)
- ORYZA SATIVA WHOLE (UNII: 84IVV0906Z)
- XYLITOL (UNII: VCQ006KQ1E)
- BEHENETH-20 (UNII: BJ4GP2IFLN)
- SODIUM ACRYLATE (UNII: 7C98FKB43H)
- SORBITAN TRISTEARATE (UNII: 6LUM696811)
- DIMETHICONE/DIENE DIMETHICONE CROSSPOLYMER (UNII: RSA9I561OK)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- MICA (UNII: V8A1AW0880)
- COCOS NUCIFERA WHOLE (UNII: 245J88W96L)
- INOSITOL (UNII: 4L6452S749)
- AMORPHOPHALLUS KONJAC ROOT (UNII: F7KU2UY3HE)
- DISODIUM EDTA-COPPER (UNII: 6V475AX06U)
- INDIGOFERA TINCTORIA LEAF (UNII: 2K7DF8HZDM)
- SERICIN 1 (UNII: N6466G03F7)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- CAMELLIA SINENSIS WHOLE (UNII: C5M4585ZBZ)
- CHONDRUS CRISPUS (UNII: OQS23HUA1X)
- AVENA SATIVA WHOLE (UNII: 5P8D0Z74RG)
- PRUNUS APETALA WHOLE (UNII: 70PO4VL8CO)
- SOPHORA FLAVESCENS WHOLE (UNII: X8KX602M5L)
- DEXTRAN 1 (UNII: I8LHQ0D645)
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- POLYGONUM ARENASTRUM WHOLE (UNII: M7IQ4O4186)
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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".