FDA.reportPublic FDA data

NerveFix

Product NDC
70163-0004
11-digit product format
701630004
Labeler code
70163
Product ID
70163-0004_82b50d4d-b8fa-4977-b91c-9e36dd46f90b
Type
HUMAN OTC DRUG
Nonproprietary name
Aconitum Napellus, Belladonna, Cantharis, Ferrum Phosphoricum, Kali Phosphoricum, Magnesia Phosphorica, Hypericum Perforatum, Spigelia Anthelmia
Dosage form
TABLET
Route
ORAL
Labeler
NaturalCare
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2026-02-03
Substance
ACONITUM NAPELLUS WHOLE; ATROPA BELLADONNA; DIBASIC POTASSIUM PHOSPHATE; FERROSOFERRIC PHOSPHATE; HYPERICUM PERFORATUM WHOLE; LYTTA VESICATORIA; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; SPIGELIA ANTHELMIA WHOLE
Active strength
6; 6; 6; 6; 12; 6; 6; 12 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
Pharmacologic classes
Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
NerveFix
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ACONITUM NAPELLUS WHOLE6 [hp_X]/1
ATROPA BELLADONNA6 [hp_X]/1
LYTTA VESICATORIA6 [hp_X]/1
FERROSOFERRIC PHOSPHATE6 [hp_X]/1
DIBASIC POTASSIUM PHOSPHATE12 [hp_X]/1
MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE6 [hp_X]/1
HYPERICUM PERFORATUM WHOLE6 [hp_X]/1
SPIGELIA ANTHELMIA WHOLE12 [hp_X]/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 8 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
U0NQ8555JDInternal UNII lookup
WQZ3G9PF0HInternal UNII lookup
3Q034RO3BTInternal UNII lookup
91GQH8I5F7Internal UNII lookup
CI71S98N1ZInternal UNII lookup
HF539G9L3QInternal UNII lookup
XK4IUX8MNBInternal UNII lookup
WYT05213GEInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
92326b54-cac9-4fb2-ae48-120a0dcbbe56Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6e3c022f-0786-43f1-8857-edff89d5153fProduct name120260309
95250459-30e4-45c1-b08a-993044f49109Product name220250805
efd58dcf-540a-4531-8766-e713129ca6f2Product name120250307
4b7700e3-6e0e-45e5-9d22-6f754d61386eProduct name220250304
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
efd58652-cb8f-4018-91ca-4b0eb2ff729fProduct name720240226
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
2641ccb3-721d-4fbf-9f2f-ca2f18157a62Product name320210309
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
e7e58cd3-cacb-49df-8d34-1ee335614abbProduct name120150609
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70163-0004-1NerveFix1 in 1 CARTONTABLET11
70163-0004-1NerveFix60 in 1 BLISTER PACKTABLET601

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
NerveFixACONITUM NAPELLUS, BELLADONNA, CANTHARIS, FERRUM PHOSPHORICUM, KALI PHOSPHORICUM, MAGNESIA PHOSPHORICA, HYPERICUM PERFORATUM, SPIGELIA ANTHELMIANaturalCare92326b54-cac9-4fb2-ae48-120a0dcbbe562026-02-03WarningsExact identifier
ndc (product): 70163-0004

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
70163-0004-1701630004011 BLISTER PACK in 1 CARTON (70163-0004-1) / 60 TABLET in 1 BLISTER PACK1 blister pack2026-02-03NoNoCurrent