Home NDC 76472-7009 Comfort Down There
Product NDC 76472-7009
11-digit product format 764727009
Labeler code 76472
Product ID 76472-7009_594f5100-8657-45a9-e063-6394a90a3ce5
Type HUMAN OTC DRUG
Nonproprietary name Aesculus hippocastanum 5C, Aloe 5C, Berberis vulgaris 3C, Capsicum Annuum 5C, Carduus marianus 3C, Nux vomica 5C, Pulsatilla 9C
Dosage form SPRAY
Route BUCCAL
Labeler SEVENE USA
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2026-08-19
Substance CAPSICUM ANNUUM WHOLE; STRYCHNOS NUX-VOMICA SEED; ALOE FEROX WHOLE; AESCULUS HIPPOCASTANUM WHOLE; BERBERIS VULGARIS ROOT BARK; PULSATILLA VULGARIS WHOLE; SILYBUM MARIANUM SEED
Active strength .1; .1; .1; .1; .1; .1; .1 mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL
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 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 Comfort Down There
Brand name suffix Hemorrhoids
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CAPSICUM ANNUUM WHOLE .1 mg/100mL STRYCHNOS NUX-VOMICA SEED .1 mg/100mL ALOE FEROX WHOLE .1 mg/100mL AESCULUS HIPPOCASTANUM WHOLE .1 mg/100mL BERBERIS VULGARIS ROOT BARK .1 mg/100mL PULSATILLA VULGARIS WHOLE .1 mg/100mL SILYBUM MARIANUM SEED .1 mg/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 7 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 Marketing start Sample Exclude flag Status 76472-7009-2 76472700902 1 BOTTLE, SPRAY in 1 BOX (76472-7009-2) / 30 mL in 1 BOTTLE, SPRAY (76472-7009-1) 2026-08-19 No No Current