BUDDATE LOTUS MOISTURE ESSENCE

Product NDC
71173-2000
11-digit product format
711732000
Labeler code
71173
Product ID
71173-2000_44cede31-8150-053d-e063-6394a90a0bc2
Type
HUMAN OTC DRUG
Nonproprietary name
Glycerin, Niacinamide, Nelumbo Nucifera Flower Extract, Portulaca Oleracea Extract
Dosage form
LIQUID
Route
TOPICAL
Labeler
BUDDATE Co Ltd
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2017-01-01
Substance
GLYCERIN; NELUMBO NUCIFERA FLOWER; NIACINAMIDE; PURSLANE
Active strength
5.93; 1.35; 2; .5 g/100mL; g/100mL; g/100mL; g/100mL
Pharmacologic classes
Allergens [CS], Cell-mediated Immunity [PE], Glycerol [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Chemical Allergen [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
BUDDATE LOTUS MOISTURE ESSENCEGLYCERIN, NIACINAMIDE, NELUMBO NUCIFERA FLOWER EXTRACT, PORTULACA OLERACEA EXTRACTBUDDATE Co Ltd46499995-8b13-3e5c-e054-00144ff88e882025-11-30WarningsExact identifier
ndc (product): 71173-2000

Additional Listing Data#

Finished product
Yes
Brand name base
BUDDATE LOTUS MOISTURE ESSENCE
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
PURSLANE5.93 g/100mL
NIACINAMIDE1.35 g/100mL
GLYCERIN2 g/100mL
NELUMBO NUCIFERA FLOWER.5 g/100mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 4 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
M6S840WXG5Internal UNII lookup
25X51I8RD4Internal UNII lookup
PDC6A3C0OXInternal UNII lookup
61W322NLDVInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
46499995-8b13-3e5c-e054-00144ff88e88Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71173-2000-12025-11-30C16284748780-12cef2736-5f4a-d83d-e063-dadaa90ab31fDrug Facts
71173-2000-12025-01-30C16284748780-12cef2736-5f4a-d83d-e063-dadaa90ab31fDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71173-2000-1BUDDATE LOTUS MOISTURE ESSENCE50 mL in 1 BOTTLE, PUMPLIQUID505

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71173-2000BUDDATE LOTUS MOISTURE ESSENCE (GLYCERIN, NIACINAMIDE, NELUMBO NUCIFERA FLOWER EXTRACT, PORTULACA OLERACEA EXTRACT) LIQUID [BUDDATE CO LTD]2Current NDC, Legacy NDC, 1 package rows20190220_46499995-8b13-3e5c-e054-00144ff88e88.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71173-2000-17117320000150 mL in 1 BOTTLE, PUMP (71173-2000-1) 50 ml2017-01-010000-00-00NoNoCurrent