PAIN RELIEF CAFFEINE AND HEMP

Product NDC: 73002-321
Requested package NDC: 73002-321-01
11-digit product format: 730020321
Labeler code: 73002
Product ID: 73002-321_efb7f444-44a9-9859-e053-2995a90a6b4b
Type: HUMAN OTC DRUG
Nonproprietary name: Caffeine (Coffeinum) 6X, Hemp extract (Cannabis sativa) 2X
Dosage form: SPRAY
Route: ORAL
Labeler: Green Earth Health Inc.
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 2019-12-19
Marketing end: 0000-00-00
Substance: CAFFEINE CITRATE; CANNABIS SATIVA SUBSP. SATIVA FLOWERING TOP
Active strength: 6 [hp_X]/mL; [hp_X]/mL
Pharmacologic classes: Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Methylxanthine [EPC], Xanthines [CS]
NDC exclude flag: No
Listing certified through: 2023-12-31
Current FDA listing: Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	73002-321	73002-321-01	D	Discontinued by firm		2026-10-05

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 13 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Snapshot, Source SHA-256 table
Captured / source date	Snapshot	Source SHA-256
2025-04-01 02:39 UTC · source 2025-03-31	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	`1332a3947898…`	`d4bfe170f9cd…`

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
7dea7767-9f52-b60a-5435-33cb9cc28bae	Product name	4	20250124
6338270f-96cb-0ecb-6fbb-0a9bc78001f4	Product name	7	20250116
0ca83774-3f79-b837-5d6f-c210102f3bc8	Product name	6	20250114
41b814f3-0166-1c53-c9ef-a0794c7daf9d	Product name	3	20221110
a590be26-846c-8659-a5a1-fb25907965dc	Product name	2	20221110
2dc76302-91c0-4c35-ad78-99adfb049c4b	Product name	1	20200603
e6065d4b-5ae1-476f-a40e-f2851cbb5d2b	Product name	2	20180221
f212291f-05fe-9603-fc7e-bd73e38ce1e6	Product name	2	20161129
182f9ab4-4ab5-c449-200f-87ce2ce8e550	Product name	2	20151105
332e86c3-7875-ca6e-f934-2206d2b31996	Product name	1	20140508
56625fcc-aa34-9d30-d0e9-1c1beb37ea21	Product name	1	20140508
7dfac40f-a405-cd2e-7c06-3059ec0e1092	Product name	1	20140508
96c2be53-8e44-452d-56a2-d255b2f1af2d	Product name	1	20140508
bf8bd5f7-495f-4022-2780-7ded7ea7ea44	Product name	1	20140508
d223c173-c39b-d764-47d4-d671d3088815	Product name	1	20140508
e01133ad-4dcd-c7f3-454b-2ff569ee160a	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
Effective	Related label
2025-07-23	Drug Facts
2024-01-30	Drug Facts
2021-08-24	Drug Facts
2021-07-23	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73002-321-01	PAIN RELIEF CAFFEINE AND HEMP	28 mL in 1 BOTTLE, SPRAY	SPRAY	28		7

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73002-321	PAIN RELIEF CAFFEINE AND HEMP (CAFFEINE (COFFEINUM) 6X, HEMP EXTRACT (CANNABIS SATIVA) 2X) SPRAY [GREEN EARTH HEALTH INC.]	6	Legacy NDC, 1 package rows	20221217_ec1b75cd-6627-439d-9f59-6ecd2ac596d1.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.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
PAIN RELIEF CAFFEINE AND HEMP	CAFFEINE (COFFEINUM) 6X, HEMP EXTRACT (CANNABIS SATIVA) 2X	Green Earth Health Inc.	ec1b75cd-6627-439d-9f59-6ecd2ac596d1	2025-07-23	Warnings	Exact identifier ndc (package): 73002-321-01 ndc (product): 73002-321 ndc11 (package): 73002032101

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
U26EO4675Q	CAFFEINE CITRATE	69-22-7	CAFFEINE CITRATE
8X454SZ22D	CANNABIS SATIVA SUBSP. SATIVA FLOWERING TOP	8063-14-7	CANNABIS SATIVA SUBSP. SATIVA FLOWERING TOP

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
73002-321-01	73002032101	28 mL in 1 BOTTLE, SPRAY (73002-321-01)	28 ml	2019-12-19	0000-00-00	No	No	Current