FDA.reportPublic FDA data

Cold Armor

Product NDC
71753-1156
11-digit product format
717531156
Labeler code
71753
Product ID
71753-1156_fb97f830-fce0-4a6d-81cf-ae5d2abe5de7
Type
HUMAN OTC DRUG
Nonproprietary name
Allium Cepa, Hydrastis Canadensis, Pulsatilla (Pratensis), Dulcamara, Nux Vomica, Ferrum Phosphoricum, Gelsemium Sempervirens, Kali Bichromicum
Dosage form
SPRAY
Route
ORAL
Labeler
Ratis, LLC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2023-05-26
Substance
FERROSOFERRIC PHOSPHATE; GELSEMIUM SEMPERVIRENS ROOT; GOLDENSEAL; ONION; POTASSIUM DICHROMATE; PULSATILLA PRATENSIS WHOLE; SOLANUM DULCAMARA TOP; STRYCHNOS NUX-VOMICA SEED
Active strength
12; 12; 6; 6; 12; 6; 8; 8 [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], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS], Vegetable Proteins [CS]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Cold Armor
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ONION12 [hp_X]/mL
GOLDENSEAL12 [hp_X]/mL
PULSATILLA PRATENSIS WHOLE6 [hp_X]/mL
SOLANUM DULCAMARA TOP6 [hp_X]/mL
STRYCHNOS NUX-VOMICA SEED12 [hp_X]/mL
FERROSOFERRIC PHOSPHATE6 [hp_X]/mL
GELSEMIUM SEMPERVIRENS ROOT8 [hp_X]/mL
POTASSIUM DICHROMATE8 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 8 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
492225Q21HInternal UNII lookup
ZW3Z11D0JVInternal UNII lookup
8E272251DIInternal UNII lookup
KPS1B1162NInternal UNII lookup
269XH13919Internal UNII lookup
91GQH8I5F7Internal UNII lookup
639KR60Q1QInternal UNII lookup
T4423S18FMInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
46af3f19-055e-4025-a14e-1d6c25880f4dAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71753-1156-1Cold Armor30 mL in 1 BOTTLE, SPRAYSPRAY301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71753-1156COLD ARMOR (ALLIUM CEPA, HYDRASTIS CANADENSIS, PULSATILLA (PRATENSIS), DULCAMARA, NUX VOMICA, FERRUM PHOSPHORICUM, GELSEMIUM SEMPERVIRENS, KALI BICHROMICUM) SPRAY [RATIS, LLC]1Current NDC, 1 package rows20230527_46af3f19-055e-4025-a14e-1d6c25880f4d.zip

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
Cold ArmorALLIUM CEPA, HYDRASTIS CANADENSIS, PULSATILLA (PRATENSIS), DULCAMARA, NUX VOMICA, FERRUM PHOSPHORICUM, GELSEMIUM SEMPERVIRENS, KALI BICHROMICUMRatis, LLC46af3f19-055e-4025-a14e-1d6c25880f4d2023-05-26WarningsExact identifier
ndc (product): 71753-1156

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71753-1156-17175311560130 mL in 1 BOTTLE, SPRAY (71753-1156-1) 30 ml2023-05-26NoNoCurrent