FDA.reportPublic FDA data

EyeClear Pro

Product NDC
68703-387
11-digit product format
687030387
Labeler code
68703
Product ID
68703-387_f4d4943b-cb79-aa71-e053-2a95a90ac638
Type
HUMAN OTC DRUG
Nonproprietary name
Calc carb, Calc fluor, Causticum, Cineraria, Euphrasia, Naphthalinum, Nat mur, Phos, Quassia, Silicea
Dosage form
LIQUID
Route
ORAL
Labeler
Silver Star Brands
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2023-03-13
Substance
NAPHTHALENE; CAUSTICUM; CALCIUM FLUORIDE; SENECIO VULGARIS; OYSTER SHELL CALCIUM CARBONATE, CRUDE; SILICON DIOXIDE; SODIUM CHLORIDE; PHOSPHORUS; EUPHRASIA STRICTA; QUASSIA AMARA WOOD
Active strength
30; 30; 30; 30; 30; 30; 30; 30; 30; 30 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product
Yes
Brand name base
EyeClear Pro
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
NAPHTHALENE30 [hp_X]/59mL
CAUSTICUM30 [hp_X]/59mL
CALCIUM FLUORIDE30 [hp_X]/59mL
SENECIO VULGARIS30 [hp_X]/59mL
OYSTER SHELL CALCIUM CARBONATE, CRUDE30 [hp_X]/59mL
SILICON DIOXIDE30 [hp_X]/59mL
SODIUM CHLORIDE30 [hp_X]/59mL
PHOSPHORUS30 [hp_X]/59mL
EUPHRASIA STRICTA30 [hp_X]/59mL
QUASSIA AMARA WOOD30 [hp_X]/59mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 10 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
2166IN72UNInternal UNII lookup
DD5FO1WKFUInternal UNII lookup
O3B55K4YKIInternal UNII lookup
W6MU8IYV12Internal UNII lookup
2E32821G6IInternal UNII lookup
ETJ7Z6XBU4Internal UNII lookup
451W47IQ8XInternal UNII lookup
27YLU75U4WInternal UNII lookup
C9642I91WLInternal UNII lookup
S5249Q85HWInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
f4d4943b-cb78-aa71-e053-2a95a90ac638Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
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
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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68703-387-02EyeClear Pro59 mL in 1 BOTTLE, GLASSLIQUID591

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68703-387EYECLEAR PRO (CALC CARB, CALC FLUOR, CAUSTICUM, CINERARIA, EUPHRASIA, NAPHTHALINUM, NAT MUR, PHOS, QUASSIA, SILICEA) LIQUID [SILVER STAR BRANDS]1Current NDC, 1 package rows20230313_f4d4943b-cb78-aa71-e053-2a95a90ac638.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
EyeClear ProCALC CARB, CALC FLUOR, CAUSTICUM, CINERARIA, EUPHRASIA, NAPHTHALINUM, NAT MUR, PHOS, QUASSIA, SILICEASilver Star Brandsf4d4943b-cb78-aa71-e053-2a95a90ac6382023-02-16WarningsExact identifier
ndc (product): 68703-387

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
68703-387-026870303870259 mL in 1 BOTTLE, GLASS (68703-387-02) 59 ml2023-03-13NoNoCurrent