NDC 58133-360 Metaderm Eczema And Baby Eczema Cream
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Get all the details for National Drug Code (NDC) 58133-360 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.
Code Structure Chart
Product Details
What is NDC 58133-360?
What are the uses for Metaderm Eczema And Baby Eczema Cream?
Which are Metaderm Eczema And Baby Eczema Cream UNII Codes?
The UNII codes for the active ingredients in this product are:
- MATRICARIA CHAMOMILLA FLOWERING TOP OIL (UNII: SA8AR2W4ER)
- MATRICARIA CHAMOMILLA FLOWERING TOP OIL (UNII: SA8AR2W4ER) (Active Moiety)
- SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508)
- SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508) (Active Moiety)
- ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK)
- ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK) (Active Moiety)
- BERBERIS VULGARIS FRUIT (UNII: 6XEF22AHC3)
- BERBERIS VULGARIS FRUIT (UNII: 6XEF22AHC3) (Active Moiety)
- CONIUM MACULATUM FRUIT (UNII: Y71WKJ3A2K)
- CONIUM MACULATUM FRUIT (UNII: Y71WKJ3A2K) (Active Moiety)
- RHUS SPP. WHOLE (UNII: 3U7FG9T9MW)
- RHUS SPP. WHOLE (UNII: 3U7FG9T9MW) (Active Moiety)
- PHYTOLACCA OCTANDRA LEAF (UNII: 0804KD28Q9)
- PHYTOLACCA OCTANDRA LEAF (UNII: 0804KD28Q9) (Active Moiety)
- AESCULUS HIPPOCASTANUM SEED OIL (UNII: E0M52HIR1Y)
- AESCULUS HIPPOCASTANUM SEED OIL (UNII: E0M52HIR1Y) (Active Moiety)
Which are Metaderm Eczema And Baby Eczema 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:
- CARTHAMUS TINCTORIUS (SAFFLOWER) OLEOSOMES (UNII: 9S60Q72309)
- VERONICA OFFICINALIS LEAF (UNII: 96R87REA55)
- ALTHAEA OFFICINALIS LEAF (UNII: E2QQV92338)
- SCROPHULARIA NODOSA (UNII: 7H443NUB2T)
- WATER (UNII: 059QF0KO0R)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TRIETHANOLAMINE LAURYLAMINOPROPIONATE (UNII: 793J74ICPW)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CARBOMER 940 (UNII: 4Q93RCW27E)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- HYDRASTIS CANADENSIS WHOLE (UNII: R763EBH88T)
- LENS CULINARIS FRUIT (UNII: ZYZ076G9JH)
- SAMBUCUS NIGRA FLOWER OIL (UNII: Q35633V53D)
- MALVA SYLVESTRIS LEAF (UNII: 17H39B00T5)
- TUSSILAGO FARFARA (UNII: 0JXZ63016V)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- NIACINAMIDE (UNII: 25X51I8RD4)
- PYRROLIDONE CARBOXYLIC ACID (UNII: 6VT1YZM21H)
- AVENA SATIVA LEAF (UNII: 206PI19V7R)
- POPULUS TREMULOIDES LEAF (UNII: 7IIH57D9E0)
- POPULUS ALBA LEAF (UNII: A74CT64437)
- COCHLEARIA OFFICINALIS LEAF (UNII: WAG1VW36J6)
- SARSAPARILLA (UNII: 2H1576D5WG)
- NASTURTIUM OFFICINALE (UNII: YH89GMV676)
- VINCETOXICUM ATRATUM ROOT (UNII: 7DQZ24B35Y)
- PIMPINELLA SAXIFRAGA ROOT (UNII: 5Y05905N7G)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- PETROLATUM (UNII: 4T6H12BN9U)
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[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".