FDA.reportPublic FDA data

Headache Ease

Product NDC
68703-374
11-digit product format
687030374
Labeler code
68703
Product ID
68703-374_2ab0f66a-fdb4-1f10-e063-6294a90af7bc
Type
HUMAN OTC DRUG
Nonproprietary name
Aur met, Belladonna, Bryonia, Gelseisum, Ignatia, Kali phos, Nat mur, Nux vom, Sepia
Dosage form
TABLET
Route
ORAL
Labeler
Silver Star Brands
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2021-12-20
Substance
ATROPA BELLADONNA; BRYONIA ALBA ROOT; GELSEMIUM SEMPERVIRENS ROOT; GOLD; POTASSIUM PHOSPHATE, DIBASIC; SEPIA OFFICINALIS JUICE; SODIUM CHLORIDE; STRYCHNOS IGNATII SEED; STRYCHNOS NUX-VOMICA SEED
Active strength
12; 12; 12; 12; 12; 12; 12; 12; 12 [hp_C]/1801; [hp_C]/1801; [hp_C]/1801; [hp_C]/1801; [hp_C]/1801; [hp_C]/1801; [hp_C]/1801; [hp_C]/1801; [hp_C]/1801
Pharmacologic classes
Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS], Standardized Chemical Allergen [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Headache Ease
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
STRYCHNOS NUX-VOMICA SEED12 [hp_C]/1801
POTASSIUM PHOSPHATE, DIBASIC12 [hp_C]/1801
SEPIA OFFICINALIS JUICE12 [hp_C]/1801
ATROPA BELLADONNA12 [hp_C]/1801
GOLD12 [hp_C]/1801
GELSEMIUM SEMPERVIRENS ROOT12 [hp_C]/1801
STRYCHNOS IGNATII SEED12 [hp_C]/1801
BRYONIA ALBA ROOT12 [hp_C]/1801
SODIUM CHLORIDE12 [hp_C]/1801

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 9 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
269XH13919Internal UNII lookup
CI71S98N1ZInternal UNII lookup
QDL83WN8C2Internal UNII lookup
WQZ3G9PF0HInternal UNII lookup
79Y1949PYOInternal UNII lookup
639KR60Q1QInternal UNII lookup
1NM3M2487KInternal UNII lookup
T7J046YI2BInternal UNII lookup
451W47IQ8XInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
c689fb16-6200-ac94-e053-2995a90a703dAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
efd58dcf-540a-4531-8766-e713129ca6f2Product name120250307
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
4b7700e3-6e0e-45e5-9d22-6f754d61386eProduct name220250304
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
bed0530e-f939-4541-956b-6928a2f6404fProduct name120241008
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name620240814
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name220171212
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68703-374-802023-12-26C16284748780-1f386c649-b895-0266-e053-dadaa90a7c1aNativeRemedies® Headache Ease Tablets
68703-374-802023-01-30C16284748780-1f386c649-b895-0266-e053-dadaa90a7c1aNativeRemedies® Headache Ease Tablets

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68703-374-80Headache Ease180 in 1 BOTTLE, GLASSTABLET1804

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68703-374HEADACHE EASE (AUR MET, BELLADONNA, BRYONIA, GELSEISUM, IGNATIA, KALI PHOS, NAT MUR, NUX VOM, SEPIA) TABLET [SILVER STAR BRANDS]4Current NDC, Legacy NDC, 1 package rows20250103_c689fb16-6200-ac94-e053-2995a90a703d.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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Headache EaseAUR MET, BELLADONNA, BRYONIA, GELSEISUM, IGNATIA, KALI PHOS, NAT MUR, NUX VOM, SEPIASilver Star Brandsc689fb16-6200-ac94-e053-2995a90a703d2025-01-01WarningsExact identifier
ndc (product): 68703-374

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68703-374-8068703037480180 TABLET in 1 BOTTLE, GLASS (68703-374-80) 180 tablet2021-12-200000-00-00NoNoCurrent