NDC 16903-170 Thera Derm
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 16903 - Manna Omni International Incorporated
- 16903-170 - Thera Derm
Product Characteristics
Product Packages
NDC Code 16903-170-03
Package Description: 240 mg in 1 BOTTLE
Product Details
What is NDC 16903-170?
What are the uses for Thera Derm?
Which are Thera Derm UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAMPHOR LEAF OIL (UNII: 51D0RGY52V)
- CAMPHOR LEAF OIL (UNII: 51D0RGY52V) (Active Moiety)
- 7-AMINODESACETOXYCEPHALOSPORANIC ACID (UNII: ANM3MSM8TN)
- 7-AMINODESACETOXYCEPHALOSPORANIC ACID (UNII: ANM3MSM8TN) (Active Moiety)
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (Active Moiety)
- METHYL SALICYLATE 2-ETHYLBUTYRATE (UNII: J8D9175Q0G)
- METHYL SALICYLATE 2-ETHYLBUTYRATE (UNII: J8D9175Q0G) (Active Moiety)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- PEPPERMINT (UNII: V95R5KMY2B) (Active Moiety)
Which are Thera Derm 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:
- PAEONIA LACTIFLORA FLOWER (UNII: R73687A534)
- SALVIA MILTIORRHIZA ROOT (UNII: 1693AM5SBN)
- ANGELICA SINENSIS ROOT OIL (UNII: T8CL3168L1)
- LIGUSTICUM SINENSE SUBSP. CHUANXIONG ROOT (UNII: RR83T99U97)
- 12-HYDROXYSTEARIC ACID (UNII: 933ANU3H2S)
- MYRRH OIL (UNII: H74221J5J4)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- PERSICARIA FILIFORMIS FLOWERING TOP (UNII: M4VKX9Q8AJ)
- NOTOPTERYGIUM INCISUM ROOT (UNII: 5Z2WW4J6RI)
- ANGELICA PUBESCENS ROOT (UNII: 0MF1EI01KJ)
- ZINGIBER CASSUMUNAR ROOT OIL (UNII: O47HX41O6C)
- COCONUT OIL (UNII: Q9L0O73W7L)
- ALOE (UNII: V5VD430YW9)
- CARTHAMUS TINCTORIUS FLOWER OIL (UNII: SDQ136WIM5)
- FRANKINCENSE OIL (UNII: 67ZYA5T02K)
* 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".