A01 CELLULAR RECHARGE

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: A01 CELLULAR RECHARGE
Generic name: ACETICUM ACIDUM, ARNICA MONTANA, AVENA SATIVA, CALCAREA CARBONICA, CALCAREA PHOSPHORICA, CALCAREA SULPHURICA, CEANOTHUS AMERICANUS, CERATOSTIGMA ILLMOTTIANUM, CHININUM ARSENICOSUM, CITRICUM ACIDUM, ENGLISH ELM, EUROPEAN HORNBEAM, EUROPEAN OLIVE, GENTIANELLA AMARELLA, HYDROFLUORICUM ACIDUM, JUGLANS REGIA, LACTICUM ACIDUM, MAGNESIA PHOSPHORICA, NATRUM MURIATICUM, NATRUM PHOSPHORICUM, NATRUM SILICOFLUORICUM, NATRUM SULPHURICUM, PASSIFLORA INCARNATA, PHOSPHORICUM ACIDUM, SARCOLACTICUM ACIDUM, SOLIDAGO VIRGAUREA
Manufacturer: Apex Energetics Inc.
Product type: HUMAN OTC DRUG
SPL set ID: b932ebd3-afea-6a95-e053-2995a90a2735
SPL ID: 0e7630cb-8c84-6d0e-e063-6394a90ace15
Version: 2
Effective date: 2024-01-08
Source export date: 2026-09-28
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:55:49

Harmonized routes table
Harmonized routes
SUBLINGUAL

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 · 34 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		A01 CELLULAR RECHARGE	openfda.brand_name
generic name		ACETICUM ACIDUM, ARNICA MONTANA, AVENA SATIVA, CALCAREA CARBONICA, CALCAREA PHOSPHORICA, CALCAREA SULPHURICA, CEANOTHUS AMERICANUS, CERATOSTIGMA ILLMOTTIANUM, CHININUM ARSENICOSUM, CITRICUM ACIDUM, ENGLISH ELM, EUROPEAN HORNBEAM, EUROPEAN OLIVE, GENTIANELLA AMARELLA, HYDROFLUORICUM ACIDUM, JUGLANS REGIA, LACTICUM ACIDUM, MAGNESIA PHOSPHORICA, NATRUM MURIATICUM, NATRUM PHOSPHORICUM, NATRUM SILICOFLUORICUM, NATRUM SULPHURICUM, PASSIFLORA INCARNATA, PHOSPHORICUM ACIDUM, SARCOLACTICUM ACIDUM, SOLIDAGO VIRGAUREA	openfda.generic_name
manufacturer name		Apex Energetics Inc.	openfda.manufacturer_name
ndc	package	63479-0101-1	openfda.package_ndc
ndc	product	63479-0101	openfda.product_ndc
ndc11	package	63479010101	derived:openfda.package_ndc
spl id		0e7630cb-8c84-6d0e-e063-6394a90ace15	id
spl set id		b932ebd3-afea-6a95-e053-2995a90a2735	set_id
unii		E934B3V59H	openfda.unii
unii		O80TY208ZW	openfda.unii
unii		0YPR65R21J	openfda.unii
unii		Q40Q9N063P	openfda.unii
unii		ZKH2SOY1AR	openfda.unii
unii		91D9GV0Z28	openfda.unii
unii		07YL55QKZ9	openfda.unii
unii		HF539G9L3Q	openfda.unii
unii		F9S9FFU82N	openfda.unii
unii		RGL5YE86CZ	openfda.unii
unii		451W47IQ8X	openfda.unii
unii		2E32821G6I	openfda.unii
unii		3B8D35Y7S4	openfda.unii
unii		806AV2E065	openfda.unii
unii		J3O020I532	openfda.unii
unii		25B1Y14T8N	openfda.unii
unii		42QO5P0NLM	openfda.unii
unii		TP69J995TW	openfda.unii
unii		3BA2N709NG	openfda.unii
unii		MA9CQJ3F7F	openfda.unii
unii		E4GA8884NN	openfda.unii
unii		XF417D3PSL	openfda.unii
unii		CLF5YFS11O	openfda.unii
unii		498M34P1VZ	openfda.unii
unii		5405K23S50	openfda.unii
unii		70WT22SF4B	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: If pregnant or breastfeeding , ask a health professional before use. Do not use if clear seal over the cap is broken or missing. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Stop use and ask a doctor if fatigue, irritability, cramps, exhaustion, restlessness, or other symptoms do not improve within 7 days or are accompanied by fever.

Reported adverse events (FAERS/openFDA)#

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