FDA.reportPublic FDA data

SinuFix

Product NDC
70163-0030
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
ANTIMONY POTASSIUM TARTRATE6 [hp_X]/mL
CALCIUM SULFIDE10 [hp_X]/mL
MERCURIC IODIDE12 [hp_X]/mL
POTASSIUM DICHROMATE6 [hp_X]/mL
SPONGIA OFFICINALIS SKELETON, ROASTED10 [hp_X]/mL
THUJA OCCIDENTALIS LEAFY TWIG6 [hp_X]/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiDL6OZ476V3, 1MBW07J51Q, R03O05RB0P, T4423S18FM, 1PIP394IID, 1NT28V9397

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

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
70163-0030-17016300300130 mL in 1 BOTTLE, DROPPER30 mlHistorical
70163-0030-2701630030021 BOTTLE, DROPPER in 1 CARTON (70163-0030-2) / 30 mL in 1 BOTTLE, DROPPER (70163-0030-1) 2026-04-22NoNoCurrent