NDC 59608-003 Tena
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 59608 - Sca Personal Care Inc.
- 59608-003 - Tena
Product Packages
NDC Code 59608-003-05
Package Description: 5 mL in 1 TUBE
NDC Code 59608-003-10
Package Description: 100 mL in 1 TUBE
Product Details
What is NDC 59608-003?
What are the uses for Tena?
Which are Tena UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (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:
- ACACIA DECURRENS FLOWER WAX (UNII: AU6XZE9IY9)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- GLYCERIN (UNII: PDC6A3C0OX)
- HELIANTHUS ANNUUS SEED WAX (UNII: 42DG15CHXV)
- HYDROGENATED JOJOBA OIL, RANDOMIZED (UNII: Q47ST02F58)
- MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYGLYCERIN-3 (UNII: 4A0NCJ6RD6)
- POLYGLYCERYL-3 RICINOLEATE (UNII: MZQ63P0N0W)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- SODIUM GLUCONATE (UNII: R6Q3791S76)
- SORBITAN (UNII: 6O92ICV9RU)
- SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
- TOCOPHEROL (UNII: R0ZB2556P8)
- CORN OIL (UNII: 8470G57WFM)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Tena?
- RxCUI: 1925201 - zinc oxide 10 % Topical Lotion
- RxCUI: 1925201 - zinc oxide 100 MG/ML Topical Lotion
- RxCUI: 1925201 - ZNO 100 MG/ML Topical Lotion
* 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".