NDC 68196-002 Members Mark Diaper Rash
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68196 - Sams West Inc
- 68196-002 - Members Mark Diaper Rash
Product Packages
NDC Code 68196-002-06
Package Description: 170 g in 1 TUBE
NDC Code 68196-002-07
Package Description: 170 g in 1 TUBE
Product Details
What is NDC 68196-002?
What are the uses for Members Mark Diaper Rash?
Which are Members Mark Diaper Rash 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 Members Mark Diaper Rash 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)
- MINERAL OIL (UNII: T5L8T28FGP)
- PETROLATUM (UNII: 4T6H12BN9U)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- PEG-30 DIPOLYHYDROXYSTEARATE (UNII: 9713Q0S7FO)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- GLYCERIN (UNII: PDC6A3C0OX)
- TROPOLONE (UNII: 7L6DL16P1T)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- PANTHENOL (UNII: WV9CM0O67Z)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
What is the NDC to RxNorm Crosswalk for Members Mark Diaper Rash?
- RxCUI: 349404 - zinc oxide 13 % Topical Cream
- RxCUI: 349404 - zinc oxide 130 MG/ML Topical Cream
- RxCUI: 349404 - ZNO 130 MG/ML Topical Cream
* 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".