FDA.reportPublic FDA data

Gun powder

Product NDC
0220-2351
11-digit product format
002202351
Labeler code
0220
Product ID
0220-2351_0a0d6462-bacc-faf6-e063-6294a90a02cc
Type
HUMAN OTC DRUG
Nonproprietary name
POTASSIUM NITRATE, ACTIVATED CHARCOAL, SULFUR
Dosage form
PELLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1983-03-03
Substance
ACTIVATED CHARCOAL; POTASSIUM NITRATE; SULFUR
Active strength
30; 30; 30 [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Gun powder
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ACTIVATED CHARCOAL30 [hp_C]/30[hp_C]
POTASSIUM NITRATE30 [hp_C]/30[hp_C]
SULFUR30 [hp_C]/30[hp_C]

Harmonized Identifiers#

Field, Values table
FieldValues
Unii2P3VWU3H10, RU45X2JN0Z, 70FD1KFU70

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-2351-412023-11-13C16284748780-1f386c649-c564-0266-e053-dadaa90a7c1aGun powder 30C
0220-2351-412023-01-30C16284748780-1f386c649-c564-0266-e053-dadaa90a7c1aGun powder 30C

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-2351-41Gun powder30 [hp_C] in 1 TUBEPELLET302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-2351GUN POWDER (POTASSIUM NITRATE, ACTIVATED CHARCOAL, SULFUR) PELLET [BOIRON]2Current NDC, Legacy NDC, 1 package rows20231114_85cb268d-43b4-3c6e-e053-2991aa0a050f.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-2351-410022023514130 [hp_C] in 1 TUBE (0220-2351-41) 1983-03-030000-00-00NoNoCurrent