Rosmarinus Lavandula

Product NDC
48951-8436
11-digit product format
489518436
Labeler code
48951
Product ID
48951-8436_3dd71b49-da4b-432c-e063-6294a90a002f
Type
HUMAN OTC DRUG
Nonproprietary name
Rosmarinus Lavandula
Dosage form
GEL
Route
TOPICAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
SLOE; URTICA URENS; BEEF; OSTREA EDULIS SHELL; SUS SCROFA SKIN; SUS SCROFA UMBILICAL CORD; BOS TAURUS SOMATIC NERVE; TIN; BOS TAURUS PLACENTA
Active strength
2; 5; 8; 8; 8; 8; 8; 8; 8 [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g
Pharmacologic classes
Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cells, Epidermal [EXT], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Meat Proteins [EXT], Non-Standardized Animal Skin Allergenic Extract [EPC], Non-Standardized Food Allergenic Extract [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
Rosmarinus Lavandula
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SLOE2 [hp_X]/g
URTICA URENS5 [hp_X]/g
BEEF8 [hp_X]/g
OSTREA EDULIS SHELL8 [hp_X]/g
SUS SCROFA SKIN8 [hp_X]/g
SUS SCROFA UMBILICAL CORD8 [hp_X]/g
BOS TAURUS SOMATIC NERVE8 [hp_X]/g
TIN8 [hp_X]/g
BOS TAURUS PLACENTA8 [hp_X]/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 9 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
3MLB4858X7Internal UNII lookup
IHN2NQ5OF9Internal UNII lookup
4PIB2155QPInternal UNII lookup
49OY13BE7ZInternal UNII lookup
3EM4VW6TQNInternal UNII lookup
118OYG6W3HInternal UNII lookup
N1R7LRU866Internal UNII lookup
387GMG9FH5Internal UNII lookup
83AL37E3A7Internal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
c3cc9a0f-7501-a0a5-e053-2995a90a767aAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-8436-5Rosmarinus Lavandula60 g in 1 TUBEGEL602

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
Rosmarinus LavandulaROSMARINUS LAVANDULAUriel Pharmacy Inc.c3cc9a0f-7501-a0a5-e053-2995a90a767a2025-09-02WarningsExact identifier
ndc (product): 48951-8436

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
48951-8436-54895184360560 g in 1 TUBE (48951-8436-5) 60 g2009-09-01NoNoCurrent