Home NDC 48951-2137 Bryophyllum Avena
Product NDC 48951-2137
11-digit product format 489512137
Labeler code 48951
Product ID 48951-2137_36393701-e4d5-153e-e063-6294a90ad80b
Type HUMAN OTC DRUG
Nonproprietary name Bryophyllum Avena
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy Inc
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance KALANCHOE DAIGREMONTIANA LEAF; OAT; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHOSPHORUS; SULFUR; VALERIAN
Active strength 1; 3; 7; 30; 30; 3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Grain Proteins [EXT], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Bryophyllum Avena
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OAT 3 [hp_X]/mL VALERIAN 3 [hp_X]/mL OYSTER SHELL CALCIUM CARBONATE, CRUDE 7 [hp_X]/mL PHOSPHORUS 30 [hp_X]/mL SULFUR 30 [hp_X]/mL KALANCHOE DAIGREMONTIANA LEAF 1 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 6 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 48951-2137-3 Bryophyllum Avena 60 mL in 1 BOTTLE, DROPPER LIQUID 60 5
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded OAT ACTIVE INGREDIENT Z6J799EAJK BRYOPHYLLUM AVENA TENSION RELIEF (OAT VALERIAN ROOT OYSTER SHELL CALCIUM CARBONATE, CRUDE PHOSPHORUS SULFUR) LIQUID [URIEL PHARMACY INC] 1 OYSTER SHELL CALCIUM CARBONATE, CRUDE ACTIVE INGREDIENT 2E32821G6I BRYOPHYLLUM AVENA TENSION RELIEF (OAT VALERIAN ROOT OYSTER SHELL CALCIUM CARBONATE, CRUDE PHOSPHORUS SULFUR) LIQUID [URIEL PHARMACY INC] 1 PHOSPHORUS ACTIVE INGREDIENT 27YLU75U4W BRYOPHYLLUM AVENA TENSION RELIEF (OAT VALERIAN ROOT OYSTER SHELL CALCIUM CARBONATE, CRUDE PHOSPHORUS SULFUR) LIQUID [URIEL PHARMACY INC] 1 SULFUR ACTIVE INGREDIENT 70FD1KFU70 BRYOPHYLLUM AVENA TENSION RELIEF (OAT VALERIAN ROOT OYSTER SHELL CALCIUM CARBONATE, CRUDE PHOSPHORUS SULFUR) LIQUID [URIEL PHARMACY INC] 1 VALERIAN ROOT ACTIVE INGREDIENT 4M98M04Z3Z BRYOPHYLLUM AVENA TENSION RELIEF (OAT VALERIAN ROOT OYSTER SHELL CALCIUM CARBONATE, CRUDE PHOSPHORUS SULFUR) LIQUID [URIEL PHARMACY INC] 1 OAT ACTIVE MOIETY Z6J799EAJK BRYOPHYLLUM AVENA TENSION RELIEF (OAT VALERIAN ROOT OYSTER SHELL CALCIUM CARBONATE, CRUDE PHOSPHORUS SULFUR) LIQUID [URIEL PHARMACY INC] 1 OYSTER SHELL CALCIUM CARBONATE, CRUDE ACTIVE MOIETY 2E32821G6I BRYOPHYLLUM AVENA TENSION RELIEF (OAT VALERIAN ROOT OYSTER SHELL CALCIUM CARBONATE, CRUDE PHOSPHORUS SULFUR) LIQUID [URIEL PHARMACY INC] 1 PHOSPHORUS ACTIVE MOIETY 27YLU75U4W BRYOPHYLLUM AVENA TENSION RELIEF (OAT VALERIAN ROOT OYSTER SHELL CALCIUM CARBONATE, CRUDE PHOSPHORUS SULFUR) LIQUID [URIEL PHARMACY INC] 1 SULFUR ACTIVE MOIETY 70FD1KFU70 BRYOPHYLLUM AVENA TENSION RELIEF (OAT VALERIAN ROOT OYSTER SHELL CALCIUM CARBONATE, CRUDE PHOSPHORUS SULFUR) LIQUID [URIEL PHARMACY INC] 1 VALERIAN ROOT ACTIVE MOIETY 4M98M04Z3Z BRYOPHYLLUM AVENA TENSION RELIEF (OAT VALERIAN ROOT OYSTER SHELL CALCIUM CARBONATE, CRUDE PHOSPHORUS SULFUR) LIQUID [URIEL PHARMACY INC] 1 GLYCERIN INACTIVE INGREDIENT PDC6A3C0OX BRYOPHYLLUM AVENA TENSION RELIEF (OAT VALERIAN ROOT OYSTER SHELL CALCIUM CARBONATE, CRUDE PHOSPHORUS SULFUR) LIQUID [URIEL PHARMACY INC] 1 WATER INACTIVE INGREDIENT 059QF0KO0R BRYOPHYLLUM AVENA TENSION RELIEF (OAT VALERIAN ROOT OYSTER SHELL CALCIUM CARBONATE, CRUDE PHOSPHORUS SULFUR) LIQUID [URIEL PHARMACY INC] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-2137 BRYOPHYLLUM AVENA LIQUID [URIEL PHARMACY INC] 4 Current NDC, Legacy NDC, 1 package rows 20240118_f3d21630-0a99-11df-8a39-0800200c9a66.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 48951-2137-3 48951213703 60 mL in 1 BOTTLE, DROPPER (48951-2137-3) 60 ml 2009-09-01 0000-00-00 No No Current