NDC 60512-9212 Cough And Cold Nighttime Formula Kids Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 60512 - Homeolab Usa Inc
- 60512-9212 - Cough And Cold Nighttime Formula Kids Relief
Product Packages
NDC Code 60512-9212-4
Package Description: 1 BOTTLE in 1 CARTON / 30 mL in 1 BOTTLE
NDC Code 60512-9212-5
Package Description: 1 BOTTLE in 1 CARTON / 100 mL in 1 BOTTLE
NDC Code 60512-9212-9
Package Description: 1 BOTTLE in 1 CARTON / 250 mL in 1 BOTTLE
Product Details
What is NDC 60512-9212?
What are the uses for Cough And Cold Nighttime Formula Kids Relief?
Which are Cough And Cold Nighttime Formula Kids Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- DROSERA ROTUNDIFOLIA FLOWERING TOP (UNII: 75O014T1HG)
- DROSERA ROTUNDIFOLIA FLOWERING TOP (UNII: 75O014T1HG) (Active Moiety)
- ARNICA MONTANA (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
- CETRARIA ISLANDICA SUBSP. ISLANDICA (UNII: BJ7YPN79A1)
- CETRARIA ISLANDICA SUBSP. ISLANDICA (UNII: BJ7YPN79A1) (Active Moiety)
- PROTORTONIA CACTI (UNII: LZB7TFX1LT)
- PROTORTONIA CACTI (UNII: LZB7TFX1LT) (Active Moiety)
- CORALLIUM RUBRUM EXOSKELETON (UNII: 2CA71K0DLE)
- CORALLIUM RUBRUM EXOSKELETON (UNII: 2CA71K0DLE) (Active Moiety)
- TIN (UNII: 387GMG9FH5)
- TIN (UNII: 387GMG9FH5) (Active Moiety)
- MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ)
- MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ) (Active Moiety)
- ARABICA COFFEE BEAN (UNII: 3SW678MX72)
- ARABICA COFFEE BEAN (UNII: 3SW678MX72) (Active Moiety)
Which are Cough And Cold Nighttime Formula Kids 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:
- WATER (UNII: 059QF0KO0R)
- SORBITOL (UNII: 506T60A25R)
- CARAMEL (UNII: T9D99G2B1R)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
* 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".