Prime of Life

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Prime of Life
Generic name: AGNUS, ALLIUM SATIVUM, AMBRA, ANGELICA SINENSIS RADIX, ARALIA QUINQUEFOLIA, ARNICA, ARSENICUM ALB., AVENA, BAPTISIA, BARYTA CARB., BRYONIA, CANTHARIS, LACHESIS, LYCOPODIUM, NUX VOM., PHOSPHORICUM AC., PULSATILLA, RUTA, SABAL, SELENIUM, ZINC. MET., GINKGO
Manufacturer: Newton Laboratories, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 99751ba5-77c2-2e89-e053-2a95a90a1269
SPL ID: b5e35e91-1a9e-8b4e-e053-2a95a90a7bff
Version: 2
Effective date: 2020-12-07
Source export date: 2026-09-28
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:28:08

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 30 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Prime of Life	openfda.brand_name
generic name		AGNUS, ALLIUM SATIVUM, AMBRA, ANGELICA SINENSIS RADIX, ARALIA QUINQUEFOLIA, ARNICA, ARSENICUM ALB., AVENA, BAPTISIA, BARYTA CARB., BRYONIA, CANTHARIS, LACHESIS, LYCOPODIUM, NUX VOM., PHOSPHORICUM AC., PULSATILLA, RUTA, SABAL, SELENIUM, ZINC. MET., GINKGO	openfda.generic_name
manufacturer name		Newton Laboratories, Inc.	openfda.manufacturer_name
ndc	package	55714-4763-1	openfda.package_ndc
ndc	product	55714-4763	openfda.product_ndc
ndc11	package	55714476301	derived:openfda.package_ndc
spl id		b5e35e91-1a9e-8b4e-e053-2a95a90a7bff	id
spl set id		99751ba5-77c2-2e89-e053-2a95a90a1269	set_id
unii		V1V998DC17	openfda.unii
unii		J7WWH9M8QS	openfda.unii
unii		269XH13919	openfda.unii
unii		8W75VCV53Q	openfda.unii
unii		O80TY208ZW	openfda.unii
unii		6P669D8HQ8	openfda.unii
unii		N94C2U587S	openfda.unii
unii		3Q034RO3BT	openfda.unii
unii		S7V92P67HO	openfda.unii
unii		XTC0D02P6C	openfda.unii
unii		433OSF3U8A	openfda.unii
unii		T7J046YI2B	openfda.unii
unii		B66F4574UG	openfda.unii
unii		VSW71SS07I	openfda.unii
unii		19FUJ2C58T	openfda.unii
unii		MA9CQJ3F7F	openfda.unii
unii		E4GA8884NN	openfda.unii
unii		5EF0HWI5WU	openfda.unii
unii		J41CSQ7QDS	openfda.unii
unii		I76KB35JEV	openfda.unii
unii		C88X29Y479	openfda.unii
unii		H6241UJ22B	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS SECTION WARNINGS: Keep out of reach of children. Do not use if tamper-evident seal is broken or missing. If symptoms worsen or persist for more than a few days, consult a doctor. If pregnant or breast-feeding , ask a doctor before use.

Reported adverse events (FAERS/openFDA)#

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