NDC 57955-2030 Heart Ache
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 57955-2030?
What are the uses for Heart Ache?
Which are Heart Ache UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALOE (UNII: V5VD430YW9)
- ALOE (UNII: V5VD430YW9) (Active Moiety)
- AMBERGRIS (UNII: XTC0D02P6C)
- AMBERGRIS (UNII: XTC0D02P6C) (Active Moiety)
- AMMONIUM CHLORIDE (UNII: 01Q9PC255D)
- AMMONIUM CATION (UNII: 54S68520I4) (Active Moiety)
- ANTIMONY TRISULFIDE (UNII: F79059A38U)
- ANTIMONY TRISULFIDE (UNII: F79059A38U) (Active Moiety)
- GOLD (UNII: 79Y1949PYO)
- GOLD (UNII: 79Y1949PYO) (Active Moiety)
- BORAGE (UNII: PB618V0K2W)
- BORAGE (UNII: PB618V0K2W) (Active Moiety)
- CICHORIUM INTYBUS FLOWER (UNII: HW54500A89)
- CICHORIUM INTYBUS FLOWER (UNII: HW54500A89) (Active Moiety)
- BLACK COHOSH (UNII: K73E24S6X9)
- BLACK COHOSH (UNII: K73E24S6X9) (Active Moiety)
- ERIODICTYON CALIFORNICUM LEAF (UNII: 2Y7TIQ135H)
- ERIODICTYON CALIFORNICUM LEAF (UNII: 2Y7TIQ135H) (Active Moiety)
- STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K)
- STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K) (Active Moiety)
- ILEX AQUIFOLIUM FLOWERING TOP (UNII: 5ENR9SAN1W)
- ILEX AQUIFOLIUM FLOWERING TOP (UNII: 5ENR9SAN1W) (Active Moiety)
- IODINE (UNII: 9679TC07X4)
- IODINE (UNII: 9679TC07X4) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
- PHOSPHORIC ACID (UNII: E4GA8884NN)
- PHOSPHORIC ACID (UNII: E4GA8884NN) (Active Moiety)
- ROSA DAMASCENA FLOWERING TOP (UNII: 21W82Q764G)
- ROSA DAMASCENA FLOWERING TOP (UNII: 21W82Q764G) (Active Moiety)
- TIN (UNII: 387GMG9FH5)
- TIN (UNII: 387GMG9FH5) (Active Moiety)
- TILIA X EUROPAEA FLOWER (UNII: NHV2K1OUDH)
- TILIA X EUROPAEA FLOWER (UNII: NHV2K1OUDH) (Active Moiety)
Which are Heart Ache 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)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
* 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".