FDA.reportPublic FDA data

Ring Relief PM Nighttime Formula

Product NDC
17312-175
11-digit product format
173120175
Labeler code
17312
Product ID
17312-175_46065bc3-19db-9699-e063-6394a90a386f
Type
HUMAN OTC DRUG
Nonproprietary name
Arnica Montana, Calcium Sulfide, Hypericum Perforatum, Lycopodium Clavatum Spore, Thiosinaminum, Mercurius Solubilis, Salicylic Acid, Silicon Dioxide, Allylthiourea
Dosage form
LIQUID
Route
AURICULAR (OTIC)
Labeler
TRP Company
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2019-09-19
Substance
ALLYLTHIOUREA; ARNICA MONTANA; CALCIUM SULFIDE; HYPERICUM PERFORATUM; LYCOPODIUM CLAVATUM SPORE; MATRICARIA CHAMOMILLA; PASSIFLORA INCARNATA FLOWER; SALICYLIC ACID; SILICON DIOXIDE; VALERIAN
Active strength
6; 6; 13; 6; 12; 12; 5; 6; 13; 6 [hp_X]/mL; [hp_X]/mL; [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
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Ring Relief PM Nighttime Formula
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ARNICA MONTANA6 [hp_X]/mL
CALCIUM SULFIDE6 [hp_X]/mL
HYPERICUM PERFORATUM13 [hp_X]/mL
LYCOPODIUM CLAVATUM SPORE6 [hp_X]/mL
MATRICARIA CHAMOMILLA12 [hp_X]/mL
SALICYLIC ACID12 [hp_X]/mL
SILICON DIOXIDE5 [hp_X]/mL
VALERIAN6 [hp_X]/mL
ALLYLTHIOUREA13 [hp_X]/mL
PASSIFLORA INCARNATA FLOWER6 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 10 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
O80TY208ZWInternal UNII lookup
1MBW07J51QInternal UNII lookup
XK4IUX8MNBInternal UNII lookup
C88X29Y479Internal UNII lookup
G0R4UBI2ZZInternal UNII lookup
O414PZ4LPZInternal UNII lookup
ETJ7Z6XBU4Internal UNII lookup
JWF5YAW3QWInternal UNII lookup
706IDJ14B7Internal UNII lookup
K8F3G29S6ZInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
92ef0dd1-84f9-086c-e053-2a95a90ac647Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17312-175-15Ring Relief PM Nighttime Formula10 mL in 1 BOTTLE, DROPPERLIQUID105
17312-175-15Ring Relief PM Nighttime Formula1 in 1 PACKAGELIQUID15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17312-175RING RELIEF PM NIGHTTIME FORMULA (ARNICA MONTANA, CALCIUM SULFIDE, HYPERICUM PERFORATUM, LYCOPODIUM CLAVATUM SPORE, THIOSINAMINUM, MERCURIUS SOLUBILIS, SALICYLIC ACID, SILICON DIOXIDE, ALLYLTHIOUREA) LIQUID [TRP COMPANY]4Current NDC, Legacy NDC, 2 package rows20240307_92ef0dd1-84f9-086c-e053-2a95a90ac647.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
Ring Relief PM Nighttime FormulaARNICA MONTANA, CALCIUM SULFIDE, HYPERICUM PERFORATUM, LYCOPODIUM CLAVATUM SPORE, THIOSINAMINUM, MERCURIUS SOLUBILIS, SALICYLIC ACID, SILICON DIOXIDE, ALLYLTHIOUREATRP Company92ef0dd1-84f9-086c-e053-2a95a90ac6472025-12-15WarningsExact identifier
ndc (product): 17312-175

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
17312-175-15173120175151 BOTTLE, DROPPER in 1 PACKAGE (17312-175-15) / 10 mL in 1 BOTTLE, DROPPER2019-09-190000-00-00NoNoCurrent