NDC 61220-001 Hydraday
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
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Product Details
What is NDC 61220-001?
What are the uses for Hydraday?
Which are Hydraday UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are Hydraday 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)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- GLYCERIN (UNII: PDC6A3C0OX)
- SESAME OIL (UNII: QX10HYY4QV)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ARGANIA SPINOSA WHOLE (UNII: 83K6O4FR76)
- ISOMALT (UNII: S870P55O2W)
- EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- MALUS DOMESTICA WHOLE (UNII: 04W636S1V3)
- XANTHAN GUM (UNII: TTV12P4NEE)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- BORAGO OFFICINALIS SEED (UNII: 2GXJ790US0)
- GLUCONOLACTONE (UNII: WQ29KQ9POT)
- ROSA CANINA FRUIT OIL (UNII: CR7307M3QZ)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SHEA BUTTER (UNII: K49155WL9Y)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- CHAMOMILE FLOWER OIL (UNII: 60F80Z61A9)
- JOJOBA OIL (UNII: 724GKU717M)
- TRIETHYLENE GLYCOL (UNII: 3P5SU53360)
- DIAMOND (UNII: 6GRV67N0U2)
- EVENING PRIMROSE OIL (UNII: 3Q9L08K71N)
- TOCOPHEROL (UNII: R0ZB2556P8)
* 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".