NDC 59779-542 Colic Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 59779 - Cvs Pharmacy
- 59779-542 - Colic Relief
Product Packages
NDC Code 59779-542-01
Package Description: 1 BOTTLE, WITH APPLICATOR in 1 CARTON / 59 mL in 1 BOTTLE, WITH APPLICATOR
Product Details
What is NDC 59779-542?
What are the uses for Colic Relief?
Which are Colic Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALOE (UNII: V5VD430YW9)
- ALOE (UNII: V5VD430YW9) (Active Moiety)
- ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)
- ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (Active Moiety)
- CARAWAY SEED (UNII: W2FH8O2BBE)
- CARAWAY SEED (UNII: W2FH8O2BBE) (Active Moiety)
- MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ)
- MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ) (Active Moiety)
- FENNEL SEED (UNII: G3QC02NIE6)
- FENNEL SEED (UNII: G3QC02NIE6) (Active Moiety)
- MELISSA OFFICINALIS (UNII: YF70189L0N)
- MELISSA OFFICINALIS (UNII: YF70189L0N) (Active Moiety)
- MENTHA PIPERITA (UNII: 79M2M2UDA9)
- MENTHA PIPERITA (UNII: 79M2M2UDA9) (Active Moiety)
- PRUNUS SPINOSA FLOWER BUD (UNII: 53Y84VPS2W)
- PRUNUS SPINOSA FLOWER BUD (UNII: 53Y84VPS2W) (Active Moiety)
- GINGER (UNII: C5529G5JPQ)
- GINGER (UNII: C5529G5JPQ) (Active Moiety)
Which are Colic Relief 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:
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- GLYCERIN (UNII: PDC6A3C0OX)
- POTASSIUM BENZOATE (UNII: 763YQN2K7K)
- POTASSIUM CITRATE (UNII: EE90ONI6FF)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- WATER (UNII: 059QF0KO0R)
- XYLITOL (UNII: VCQ006KQ1E)
* 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".