SinuFix

Product NDC
70163-0030
Requested package NDC
70163-0030-2
11-digit product format
701630030
Labeler code
70163
Product ID
70163-0030_fbd27f97-5014-489e-8d3a-1475247f8b4d
Type
HUMAN OTC DRUG
Nonproprietary name
Thuja Occidentalis, Antimonium Tartaricum, Kali Bichromicum, Mercurius Iodatus Ruber, Spongia Tosta, Hepar Sulphuris Calcareum
Dosage form
LIQUID
Route
ORAL
Labeler
NaturalCare
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2026-04-22
Substance
ANTIMONY POTASSIUM TARTRATE; CALCIUM SULFIDE; MERCURIC IODIDE; POTASSIUM DICHROMATE; SPONGIA OFFICINALIS SKELETON, ROASTED; THUJA OCCIDENTALIS LEAFY TWIG
Active strength
6; 10; 12; 6; 10; 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
SinuFix
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
THUJA OCCIDENTALIS LEAFY TWIG6 [hp_X]/mL
ANTIMONY POTASSIUM TARTRATE10 [hp_X]/mL
POTASSIUM DICHROMATE12 [hp_X]/mL
MERCURIC IODIDE6 [hp_X]/mL
SPONGIA OFFICINALIS SKELETON, ROASTED10 [hp_X]/mL
CALCIUM SULFIDE6 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 6 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1NT28V9397Internal UNII lookup
DL6OZ476V3Internal UNII lookup
T4423S18FMInternal UNII lookup
R03O05RB0PInternal UNII lookup
1PIP394IIDInternal UNII lookup
1MBW07J51QInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
3e2346e7-55a1-416e-b2ef-04d43e40d67fAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70163-0030-1SinuFix30 mL in 1 BOTTLE, DROPPERLIQUID301
70163-0030-2SinuFix1 in 1 CARTONLIQUID11

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
SinuFixTHUJA OCCIDENTALIS, ANTIMONIUM TARTARICUM, KALI BICHROMICUM, MERCURIUS IODATUS RUBER, SPONGIA TOSTA, HEPAR SULPHURIS CALCAREUMNaturalCare3e2346e7-55a1-416e-b2ef-04d43e40d67f2026-04-22WarningsExact identifier
ndc (package): 70163-0030-2
ndc (product): 70163-0030
ndc11 (package): 70163003002

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
70163-0030-2701630030021 BOTTLE, DROPPER in 1 CARTON (70163-0030-2) / 30 mL in 1 BOTTLE, DROPPER (70163-0030-1) 2026-04-22NoNoCurrent