FDA.reportPublic FDA data

CHESTAL COUGH AND MUCUS

Product NDC
0220-9115
11-digit product format
002209115
Labeler code
0220
Product ID
0220-9115_4d77a058-e6c9-2af5-e063-6394a90afe1a
Type
HUMAN OTC DRUG
Nonproprietary name
ANTIMONY POTASSIUM TARTRATE, BRYONIA ALBA ROOT, PROTORTONIA CACTI, DROSERA ROTUNDIFOLIA, IPECAC, PULSATILLA VULGARIS WHOLE, RUMEX CRISPUS ROOT, SPONGIA OFFICINALIS SKELETON, ROASTED, LOBARIA PULMONARIA
Dosage form
TABLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2026-03-20
Substance
ANTIMONY POTASSIUM TARTRATE; BRYONIA ALBA ROOT; DROSERA ROTUNDIFOLIA; IPECAC; LOBARIA PULMONARIA; PROTORTONIA CACTI; PULSATILLA VULGARIS WHOLE; RUMEX CRISPUS ROOT; SPONGIA OFFICINALIS SKELETON, ROASTED
Active strength
6; 3; 3; 3; 3; 3; 6; 6; 3 [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
CHESTAL COUGH AND MUCUS
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SPONGIA OFFICINALIS SKELETON, ROASTED6 [hp_C]/1
IPECAC3 [hp_C]/1
RUMEX CRISPUS ROOT3 [hp_C]/1
LOBARIA PULMONARIA3 [hp_C]/1
PROTORTONIA CACTI3 [hp_C]/1
DROSERA ROTUNDIFOLIA3 [hp_C]/1
PULSATILLA VULGARIS WHOLE6 [hp_C]/1
ANTIMONY POTASSIUM TARTRATE6 [hp_C]/1
BRYONIA ALBA ROOT3 [hp_C]/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 9 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1PIP394IIDInternal UNII lookup
62I3C8233LInternal UNII lookup
9N1RM2S62CInternal UNII lookup
D1YM0P5Z2TInternal UNII lookup
LZB7TFX1LTInternal UNII lookup
QR44N9XPJQInternal UNII lookup
I76KB35JEVInternal UNII lookup
DL6OZ476V3Internal UNII lookup
T7J046YI2BInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
4d77a058-e6c8-2af5-e063-6394a90afe1aAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-9115-04CHESTAL COUGH AND MUCUS20 in 1 BLISTER PACKTABLET201
0220-9115-04CHESTAL COUGH AND MUCUS3 in 1 CARTONTABLET31

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
CHESTAL COUGH AND MUCUSANTIMONY POTASSIUM TARTRATE, BRYONIA ALBA ROOT, PROTORTONIA CACTI, DROSERA ROTUNDIFOLIA, IPECAC, PULSATILLA VULGARIS WHOLE, RUMEX CRISPUS ROOT, SPONGIA OFFICINALIS SKELETON, ROASTED, LOBARIA PULMONARIABoiron4d77a058-e6c8-2af5-e063-6394a90afe1a2026-03-20WarningsExact identifier
ndc (product): 0220-9115

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
0220-9115-04002209115043 BLISTER PACK in 1 CARTON (0220-9115-04) / 20 TABLET in 1 BLISTER PACK3 blister pack2026-03-20NoNoCurrent