FDA.reportPublic FDA data

Cough and Mucus

Product NDC
70163-0036
11-digit product format
701630036
Labeler code
70163
Product ID
70163-0036_b53d460d-501e-460e-b2f6-29b280b16051
Type
HUMAN OTC DRUG
Nonproprietary name
Antimonium Tartaricum, Euphrasia Officinalis, Hepar Sulphuris Calcareum, Hydrastis Canadensis, Kali Bichromicum, Pulsatilla (Pratensis), Stannum Metallicum, Sulphur
Dosage form
LIQUID
Route
ORAL
Labeler
NaturalCare
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2026-03-23
Substance
ANTIMONY POTASSIUM TARTRATE; CALCIUM SULFIDE; EUPHRASIA STRICTA; GOLDENSEAL; POTASSIUM DICHROMATE; PULSATILLA PRATENSIS WHOLE; SULFUR; TIN
Active strength
6; 12; 6; 5; 12; 6; 12; 12 [hp_X]/mL; [hp_X]/mL; [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
Cough and Mucus
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ANTIMONY POTASSIUM TARTRATE6 [hp_X]/mL
CALCIUM SULFIDE12 [hp_X]/mL
EUPHRASIA STRICTA6 [hp_X]/mL
GOLDENSEAL5 [hp_X]/mL
POTASSIUM DICHROMATE12 [hp_X]/mL
PULSATILLA PRATENSIS WHOLE6 [hp_X]/mL
SULFUR12 [hp_X]/mL
TIN12 [hp_X]/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiDL6OZ476V3, 1MBW07J51Q, C9642I91WL, ZW3Z11D0JV, T4423S18FM, 8E272251DI, 70FD1KFU70, 387GMG9FH5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70163-0036-1Cough and Mucus120 mL in 1 BOTTLE, GLASSLIQUID1201
70163-0036-2Cough and Mucus1 in 1 CARTONLIQUID11

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
70163-0036-170163003601120 mL in 1 BOTTLE, GLASS120 mlHistorical
70163-0036-2701630036021 BOTTLE, GLASS in 1 CARTON (70163-0036-2) / 120 mL in 1 BOTTLE, GLASS (70163-0036-1) 2026-03-23NoNoCurrent