NDC 43846-0036 Hot Flash Rescue
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 43846-0036?
What are the uses for Hot Flash Rescue?
Which are Hot Flash Rescue UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAPSICUM (UNII: 00UK7646FG)
- CAPSICUM (UNII: 00UK7646FG) (Active Moiety)
- PULSATILLA VULGARIS (UNII: I76KB35JEV)
- PULSATILLA VULGARIS (UNII: I76KB35JEV) (Active Moiety)
- SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508)
- SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508) (Active Moiety)
Which are Hot Flash Rescue 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- AVOCADO OIL (UNII: 6VNO72PFC1)
- BLACK COHOSH (UNII: K73E24S6X9)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- CHASTE TREE (UNII: 433OSF3U8A)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- KUKUI NUT OIL (UNII: TP11QR7B8R)
- LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
- MACADAMIA OIL (UNII: 515610SU8C)
- OREGANO (UNII: 0E5AT8T16U)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- POLYETHYLENE GLYCOL 1500 (UNII: 1212Z7S33A)
- PEG-8 DIMETHICONE (UNII: GIA7T764OD)
- POLYETHYLENE GLYCOL 700 (UNII: 762678AC5R)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- SORBIC ACID (UNII: X045WJ989B)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- WATER (UNII: 059QF0KO0R)
- ROSA CANINA SEED (UNII: 4503R1M9UT)
- SAGE (UNII: 065C5D077J)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- DIOSCOREA VILLOSA ROOT (UNII: IWY3IWX2G8)
* 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".