NDC 59608-002 Tena
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 59608-002?
What are the uses for Tena?
Which are Tena UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Tena 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)
- DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
- GLYCERIN (UNII: PDC6A3C0OX)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- CETETH-20 (UNII: I835H2IHHX)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- SORBITAN (UNII: 6O92ICV9RU)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- JOJOBA OIL, RANDOMIZED (UNII: 7F0EV20QYL)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- STEARETH-20 (UNII: L0Q8IK9E08)
- HELIANTHUS ANNUUS SEED WAX (UNII: 42DG15CHXV)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- SODIUM GLUCONATE (UNII: R6Q3791S76)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ACACIA DECURRENS FLOWER WAX (UNII: AU6XZE9IY9)
- POLYGLYCERIN-3 (UNII: 4A0NCJ6RD6)
- TOCOPHEROL (UNII: R0ZB2556P8)
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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".