FDA.reportPublic FDA data

7th MANNA PAIN RELIEF DROPS

Product NDC
71856-423
Requested package NDC
71856-423-00
11-digit product format
718560423
Labeler code
71856
Product ID
71856-423_09dc19d0-24b9-bd12-e063-6294a90ab40f
Type
HUMAN OTC DRUG
Nonproprietary name
MENTHOL, CAMPHOR (SYNTHETIC)
Dosage form
LIQUID
Route
TOPICAL
Labeler
7TH MANNA (USA) PTE. LTD.
Application
M017B
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2023-09-25
Substance
MENTHOL; CAMPHOR (SYNTHETIC)
Active strength
100; 30 mg/mL; mg/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product
Yes
Brand name base
7th MANNA PAIN RELIEF DROPS
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MENTHOL100 mg/mL
CAMPHOR (SYNTHETIC)30 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
L7T10EIP3AInternal UNII lookup
5TJD82A1ETInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1987413Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
699c668c-4f54-4f18-b585-bdcebe7a2c4eAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71856-423-007th MANNA PAIN RELIEF DROPS1 in 1 BOXLIQUID12
71856-423-007th MANNA PAIN RELIEF DROPS30 mL in 1 BOTTLELIQUID302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71856-4237TH MANNA PAIN RELIEF DROPS (MENTHOL, CAMPHOR (SYNTHETIC)) LIQUID [7TH MANNA (USA) PTE. LTD.]2Current NDC, 2 package rows20231112_699c668c-4f54-4f18-b585-bdcebe7a2c4e.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
7th MANNA PAIN RELIEF DROPSMENTHOL, CAMPHOR (SYNTHETIC)7TH MANNA (USA) PTE. LTD.699c668c-4f54-4f18-b585-bdcebe7a2c4e2023-11-11WarningsExact identifier
ndc (package): 71856-423-00
ndc (product): 71856-423
ndc11 (package): 71856042300

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1987413camphor 3 % / menthol 10 % Topical SolutionPSN699c668c-4f54-4f18-b585-bdcebe7a2c4e2
1987413camphor 30 MG/ML / menthol 100 MG/ML Topical SolutionSCD699c668c-4f54-4f18-b585-bdcebe7a2c4e2
1987413camphor 3 % / menthol 10 % Topical SolutionSY699c668c-4f54-4f18-b585-bdcebe7a2c4e2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71856-423-00718560423001 BOTTLE in 1 BOX (71856-423-00) / 30 mL in 1 BOTTLE1 bottle2023-09-25NoNoCurrent