NDC 60541-1900 Glo Skin Beauty Remedy Gel
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 60541-1900?
What are the uses for Glo Skin Beauty Remedy Gel?
Which are Glo Skin Beauty Remedy Gel UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYDROCORTISONE (UNII: WI4X0X7BPJ)
- HYDROCORTISONE (UNII: WI4X0X7BPJ) (Active Moiety)
Which are Glo Skin Beauty Remedy Gel 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- CAPRYLIC/CAPRIC ACID (UNII: DI775RT244)
- ROSA CANINA FRUIT OIL (UNII: CR7307M3QZ)
- SQUALANE (UNII: GW89575KF9)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- .ALPHA.-BISABOLOL, (+)- (UNII: 105S6I733Z)
- CARBOMER 940 (UNII: 4Q93RCW27E)
- GLUCONOLACTONE (UNII: WQ29KQ9POT)
- LONICERA CAPRIFOLIUM FLOWER (UNII: 5N1WD9784U)
- HEDYCHIUM CORONARIUM ROOT (UNII: 92A6N0IQN9)
- LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- TOCOPHEROL (UNII: R0ZB2556P8)
- SOYBEAN OIL (UNII: 241ATL177A)
- ALOE VERA WHOLE (UNII: KIZ4X2EHYX)
- SODIUM HYDRIDE (UNII: 23J3BHR95O)
- XANTHAN GUM (UNII: TTV12P4NEE)
- TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)
What is the NDC to RxNorm Crosswalk for Glo Skin Beauty Remedy Gel?
- RxCUI: 198706 - hydrocortisone 1 % Topical Gel
- RxCUI: 198706 - hydrocortisone 0.01 MG/MG Topical Gel
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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".