STYE EYE RELIEF SERUM

Product NDC
84896-001
Requested package NDC
84896-001-01
11-digit product format
848960001
Labeler code
84896
Product ID
84896-001_46218208-8a0f-d622-e063-6394a90ab43c
Type
HUMAN OTC DRUG
Nonproprietary name
Vitamin E
Dosage form
PASTE
Route
TOPICAL
Labeler
Guangzhou Mizi Biotechnology Co., LTD.
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-09-16
Substance
ACETYL HEXAPEPTIDE-8 AMIDE; ASCORBIC ACID; PREZATIDE COPPER; ASPARTIC ACID; LYSINE
Active strength
.5; 1; .1; 2; 1 g/100mL; g/100mL; g/100mL; g/100mL; g/100mL
Pharmacologic classes
Ascorbic Acid [CS], Vitamin C [EPC]
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
STYE EYE RELIEF SERUM
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ACETYL HEXAPEPTIDE-8 AMIDE.5 g/100mL
ASCORBIC ACID1 g/100mL
PREZATIDE COPPER.1 g/100mL
ASPARTIC ACID2 g/100mL
LYSINE1 g/100mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 5 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
L4EL31FWILInternal UNII lookup
PQ6CK8PD0RInternal UNII lookup
6BJQ43T1I9Internal UNII lookup
30KYC7MIAIInternal UNII lookup
K3Z4F929H6Internal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
3f60193e-4b95-6759-e063-6394a90a991cAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84896-001-01STYE EYE RELIEF SERUM30 mL in 1 BOTTLE, DROPPERPASTE302

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
STYE EYE RELIEF SERUMVITAMIN EGuangzhou Mizi Biotechnology Co., LTD.3f60193e-4b95-6759-e063-6394a90a991c2025-12-17WarningsExact identifier
ndc (package): 84896-001-01
ndc (product): 84896-001
ndc11 (package): 84896000101

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
84896-001-018489600010130 mL in 1 BOTTLE, DROPPER (84896-001-01) 30 ml2025-09-16NoNoCurrent