Home NDC 71919-826 Graphites
Product NDC 71919-826
11-digit product format 719190826
Labeler code 71919
Product ID 71919-826_2e988182-cd12-fea7-e063-6294a90a0d1f
Type HUMAN OTC DRUG
Nonproprietary name GRAPHITE
Dosage form PELLET
Route ORAL
Labeler Washington Homeopathic Products
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2025-02-20
Substance GRAPHITE
Active strength 30 [hp_C]/1
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Graphites
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength GRAPHITE 30 [hp_C]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4QQN74LH4O 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 71919-826-05 Graphites 900 in 1 VIAL, GLASS PELLET 900 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71919-826 GRAPHITES (GRAPHITE) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS] 1 Current NDC, 1 package rows 20250223_2e988182-cd11-fea7-e063-6294a90a0d1f.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 71919-826-05 71919082605 900 PELLET in 1 VIAL, GLASS (71919-826-05) 900 pellet 2025-02-20 No No Current