Home NDC 0220-9074-09 ColicComfort
Product NDC 0220-9074
Requested package NDC 0220-9074-09
11-digit product format 002209074
Labeler code 0220
Product ID 0220-9074_1a9e144b-7444-dc58-e063-6394a90a6ca0
Type HUMAN OTC DRUG
Nonproprietary name ACTIVATED CHARCOAL, COPPER, CITRULLUS COLOCYNTHIS FRUIT
Dosage form LIQUID
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2018-09-15
Marketing end 2029-10-31
Substance ACTIVATED CHARCOAL; CITRULLUS COLOCYNTHIS FRUIT; COPPER
Active strength 5; 9; 5 [hp_C]/1; [hp_C]/1; [hp_C]/1
Pharmacologic classes Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Inhibit Ovum Fertilization [PE]
NDC exclude flag No
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 3 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2024-05-28 21:12 UTC · source 2024-05-28 excluded package package 0220-9074 0220-9074-09 I Inactivated by FDA excluded / ndc_excluded.zip 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 excluded package package 0220-9074 0220-9074-09 I Inactivated by FDA excluded / ndc_excluded.zip 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 0220-9074 0220-9074-09 I Inactivated by FDA excluded / ndc_excluded.zip 1332a3947898…d4bfe170f9cd…
Additional Listing Data#
Finished product Yes
Brand name base ColicComfort Active Ingredients# Ingredient, Strength table Ingredient Strength ACTIVATED CHARCOAL 5 [hp_C]/1 COPPER 5 [hp_C]/1 CITRULLUS COLOCYNTHIS FRUIT 9 [hp_C]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2P3VWU3H10 Internal UNII lookup 789U1901C5 Internal UNII lookup 0E49E3V9U6 Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0220-9074-09 ColicComfort 30 in 1 BOX LIQUID 30 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0220-9074 COLICCOMFORT (ACTIVATED CHARCOAL, COPPER, CITRULLUS COLOCYNTHIS FRUIT) LIQUID [BOIRON] 3 Current NDC, Legacy NDC, 1 package rows 20240612_74aa5ab4-cd93-36b0-e053-2991aa0a1068.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 0220-9074-09 00220907409 30 LIQUID in 1 BOX (0220-9074-09) 30 liquid 2018-09-15 2029-10-31 No No Current