Graphitis

Product NDC: 53645-1670
11-digit product format: 536451670
Labeler code: 53645
Product ID: 53645-1670_faa4bfea-4b7c-e530-e053-6294a90a5e5f
Type: HUMAN OTC DRUG
Nonproprietary name: Graphitis
Dosage form: GLOBULE
Route: ORAL
Labeler: True Botanica, LLC
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 2014-02-03
Substance: GRAPHITE
Active strength: 30 [hp_X]/23g
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Additional Listing Data#

Finished product: Yes
Brand name base: Graphitis
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
GRAPHITE	30 [hp_X]/23g

Harmonized Identifiers#

Field, Values table
Field	Values
Unii	4QQN74LH4O

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
53645-1670-2	2021-01-31	C162847	48780-1	ba0f9c33-170a-a910-e053-dadaa90a0b85	Graphites 30X
53645-1670-2	2021-01-29	C162847	48780-1	ba0f9c33-170a-a910-e053-dadaa90a0b85	Graphites 30X

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
53645-1670-2	Graphitis	23 g in 1 BOTTLE	GLOBULE	23		5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
53645-1670	GRAPHITIS GLOBULE [TRUE BOTANICA, LLC]	5	Current NDC, Legacy NDC, 1 package rows	20230502_61952fe1-813f-ff6e-e053-2a91aa0a2d58.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
53645-1670-2	53645167002	23 g in 1 BOTTLE (53645-1670-2)	23 g	2014-02-03	0000-00-00	No	No	Current