FDA.reportPublic FDA data

PARV Plus

Product NDC
43742-2532
11-digit product format
437422532
Labeler code
43742
Product ID
43742-2532_81d00235-5b69-4a5b-9f35-7af9fc8b6dc7
Type
HUMAN OTC DRUG
Nonproprietary name
Antimonium Crudum, Apis Mellifica, Chamomilla, Echinacea (Angustifolia), Ferrum Phosphoricum, Pulsatilla (Pratensis), Rhus Tox, Sulphur, Urtica Urens
Dosage form
LIQUID
Route
ORAL
Labeler
Deseret Biologicals, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2026-01-02
Substance
ANTIMONY TRISULFIDE; APIS MELLIFERA; MATRICARIA CHAMOMILLA WHOLE; ECHINACEA ANGUSTIFOLIA WHOLE; FERROSOFERRIC PHOSPHATE; PULSATILLA PRATENSIS WHOLE; TOXICODENDRON PUBESCENS LEAF; SULFUR; URTICA URENS WHOLE
Active strength
12; 12; 6; 6; 12; 12; 12; 12; 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes
Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Standardized Insect Venom Allergenic Extract [EPC]
NDC exclude flag
No
Listing certified through
2027-12-31
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
PARV Plus
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ANTIMONY TRISULFIDE12 [hp_X]/mL
APIS MELLIFERA12 [hp_X]/mL
MATRICARIA CHAMOMILLA WHOLE6 [hp_X]/mL
ECHINACEA ANGUSTIFOLIA WHOLE6 [hp_X]/mL
FERROSOFERRIC PHOSPHATE12 [hp_X]/mL
PULSATILLA PRATENSIS WHOLE12 [hp_X]/mL
TOXICODENDRON PUBESCENS LEAF12 [hp_X]/mL
SULFUR12 [hp_X]/mL
URTICA URENS WHOLE6 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 9 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
F79059A38UInternal UNII lookup
7S82P3R43ZInternal UNII lookup
G0R4UBI2ZZInternal UNII lookup
VB06AV5US8Internal UNII lookup
91GQH8I5F7Internal UNII lookup
8E272251DIInternal UNII lookup
6IO182RP7AInternal UNII lookup
70FD1KFU70Internal UNII lookup
IHN2NQ5OF9Internal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
187113bf-fcec-4942-8343-dc200bd3e5e9Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43742-2532-1PARV Plus30 mL in 1 BOTTLE, DROPPERLIQUID301

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
PARV PlusANTIMONIUM CRUDUM, APIS MELLIFICA, CHAMOMILLA, ECHINACEA (ANGUSTIFOLIA), FERRUM PHOSPHORICUM, PULSATILLA (PRATENSIS), RHUS TOX, SULPHUR, URTICA URENSDeseret Biologicals, Inc.187113bf-fcec-4942-8343-dc200bd3e5e92026-01-02WarningsExact identifier
ndc (product): 43742-2532

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
43742-2532-14374225320130 mL in 1 BOTTLE, DROPPER (43742-2532-1) 30 ml2026-01-02NoNoCurrent