Home NDC 68703-392-02 NativeRemedies Anger-Soothe
Product NDC 68703-392
Requested package NDC 68703-392-02
11-digit product format 687030392
Labeler code 68703
Product ID 68703-392_2ab0f66a-fdb0-1f10-e063-6294a90af7bc
Type HUMAN OTC DRUG
Nonproprietary name Chamomilla, Lycopodium, Nux vomica
Dosage form LIQUID
Route ORAL
Labeler Silver Star Brands
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2023-03-20
Substance STRYCHNOS NUX-VOMICA SEED; MATRICARIA RECUTITA; LYCOPODIUM CLAVATUM SPORE
Active strength 6; 6; 6 [hp_C]/59mL; [hp_C]/59mL; [hp_C]/59mL
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]
NDC exclude flag No
Listing certified through 2026-12-31
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 NativeRemedies Anger-Soothe
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength STRYCHNOS NUX-VOMICA SEED 6 [hp_C]/59mL MATRICARIA RECUTITA 6 [hp_C]/59mL LYCOPODIUM CLAVATUM SPORE 6 [hp_C]/59mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 269XH13919 Internal UNII lookup G0R4UBI2ZZ Internal UNII lookup C88X29Y479 Internal UNII lookup
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 68703-392-02 NativeRemedies Anger-Soothe 59 mL in 1 BOTTLE, DROPPER LIQUID 59 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68703-392 NATIVEREMEDIES ANGER-SOOTHE (CHAMOMILLA, LYCOPODIUM, NUX VOMICA) LIQUID [SILVER STAR BRANDS] 3 Current NDC, 1 package rows 20250103_f67f7955-c4e9-64d7-e053-2995a90ac756.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 Sample Exclude flag Status 68703-392-02 68703039202 59 mL in 1 BOTTLE, DROPPER (68703-392-02) 59 ml 2023-03-20 No No Current