Home NDC 48951-3216 Carbo Chamomilla
Product NDC 48951-3216
11-digit product format 489513216
Labeler code 48951
Product ID 48951-3216_5907ec1f-624e-81d5-e063-6394a90a2b91
Type HUMAN OTC DRUG
Nonproprietary name Carbo Chamomilla
Dosage form CAPSULE
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance ANTIMONY TRISULFIDE; MATRICARIA RECUTITA; WORMWOOD; GENTIANA LUTEA ROOT; ARSENIC TRIOXIDE; ACORUS CALAMUS ROOT; GEUM URBANUM ROOT; GINGER; BLACK PEPPER
Active strength 3; 3; 5; 5; 6; 6; 3; 5; 7 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
Pharmacologic classes Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Vegetable Proteins [CS]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Carbo Chamomilla
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ANTIMONY TRISULFIDE 3 [hp_X]/1 MATRICARIA RECUTITA 3 [hp_X]/1 WORMWOOD 5 [hp_X]/1 GENTIANA LUTEA ROOT 5 [hp_X]/1 ARSENIC TRIOXIDE 6 [hp_X]/1 ACORUS CALAMUS ROOT 6 [hp_X]/1 GEUM URBANUM ROOT 3 [hp_X]/1 GINGER 5 [hp_X]/1 BLACK PEPPER 7 [hp_X]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 9 matching rows.
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 48951-3216-7 Carbo Chamomilla 90 in 1 BOTTLE, GLASS CAPSULE 90 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-3216 CARBO CHAMOMILLA CAPSULE [URIEL PHARMACY INC.] 4 Current NDC, Legacy NDC, 1 package rows 20241116_6bc88bd3-ffe9-46d7-e053-2a91aa0acf79.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 48951-3216-7 48951321607 90 CAPSULE in 1 BOTTLE, GLASS (48951-3216-7) 90 capsule 2009-09-01 0000-00-00 No No Current