NDC 69003-412 Naruko Taiwan Magnolia Firming Smooth Finish Cream Makeup
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Get all the details for National Drug Code (NDC) 69003-412 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.
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Product Details
What is NDC 69003-412?
What are the uses for Naruko Taiwan Magnolia Firming Smooth Finish Cream Makeup?
Which are Naruko Taiwan Magnolia Firming Smooth Finish Cream Makeup UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Naruko Taiwan Magnolia Firming Smooth Finish Cream Makeup 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:
- DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE (UNII: ANQ870JD20)
- ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
- HYDROGENATED POLYBUTENE (1300 MW) (UNII: 7D1YQ9Y5EZ)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- SODIUM SILICATE (UNII: IJF18F77L3)
- POTASSIUM SILICATE (UNII: J86L1GUL6K)
- ALUMINUM SILICATE (UNII: T1FAD4SS2M)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- MAGNOLIA GRANDIFLORA LEAF (UNII: J4B095E3UN)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- PENTAERYTHRITYL TETRAISOSTEARATE (UNII: 9D7IK5483F)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- CARNOSINE (UNII: 8HO6PVN24W)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- KALANCHOE PINNATA LEAF (UNII: 3R963LO08T)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- SCUTELLARIA ALPINA FLOWERING TOP (UNII: 68JZ9NK55M)
- PEUCEDANUM OSTRUTHIUM LEAF (UNII: 86P27YRR6Y)
- GINKGO (UNII: 19FUJ2C58T)
- ARTEMISIA UMBELLIFORMIS WHOLE (UNII: BI6LY4V6G3)
- LEONTOPODIUM ALPINUM (UNII: 7R4LQP52DM)
- EPILOBIUM ANGUSTIFOLIUM WHOLE (UNII: C278QS9YBT)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- CHAMOMILE (UNII: FGL3685T2X)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- TREMELLA FUCIFORMIS WHOLE (UNII: 4938BNS0GU)
- MAGNOLIA X ALBA FLOWER OIL (UNII: 8QDN200R1S)
- GINGER (UNII: C5529G5JPQ)
- JUJUBE FRUIT (UNII: G55HNL2C70)
- CLOVE (UNII: K48IKT5321)
- PRUNUS MUME FRUIT (UNII: 639190I8CU)
- CNIDIUM OFFICINALE ROOT (UNII: 8S3OZD358J)
- ANGELICA ACUTILOBA ROOT (UNII: 3W51R3EK30)
- AMARANTHUS HYPOCHONDRIACUS WHOLE (UNII: YL06Y84R9Z)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- 3-O-ETHYL ASCORBIC ACID (UNII: 6MW60CB71P)
- TAGETES ERECTA WHOLE (UNII: C7YOV7LU4Q)
- OXALIS CORNICULATA WHOLE (UNII: HJ70WR4413)
- CAMELLIA JAPONICA SEED OIL (UNII: U37N0S910T)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- TREHALOSE (UNII: B8WCK70T7I)
- SORBITOL (UNII: 506T60A25R)
- GLYCERIN (UNII: PDC6A3C0OX)
- PANTHENOL (UNII: WV9CM0O67Z)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- UREA (UNII: 8W8T17847W)
- POLYQUATERNIUM-51 (2-METHACRYLOYLOXYETHYL PHOSPHORYLCHOLINE/N-BUTYL METHACRYLATE; 3:7) (UNII: EL9825H96J)
- MAGNOLIA OFFICINALIS BARK (UNII: 5M609NV974)
- OCTYLDODECYL MYRISTATE (UNII: S013N99GR8)
- COIX LACRYMA-JOBI SEED (UNII: 4Q4V6NTZ1F)
- MEADOWFOAM SEED OIL (UNII: 412ZHA4T4Y)
- LAUROYL LYSINE (UNII: 113171Q70B)
- ADANSONIA DIGITATA WHOLE (UNII: D5B40OA634)
- RAPESEED STEROL (UNII: B46B6DD20U)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- BELLIS PERENNIS FLOWER (UNII: 26I94X9A1K)
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".