FDA.reportPublic FDA data

Facial Pain Formula

Product NDC
83027-0087
11-digit product format
830270087
Labeler code
83027
Product ID
83027-0087_1328f257-44b2-4be8-b0e4-6dbad85d7361
Type
HUMAN OTC DRUG
Nonproprietary name
Salix Nigra, Belladonna, Cerebellum (Suis), Aconitum Napellus
Dosage form
SPRAY
Route
ORAL
Labeler
Nutritional Specialties, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2023-07-06
Substance
ACONITUM NAPELLUS WHOLE; ATROPA BELLADONNA; SALIX NIGRA BARK; SUS SCROFA CEREBELLUM
Active strength
8; 6; 3; 6 [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
Facial Pain Formula
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ACONITUM NAPELLUS WHOLE8 [hp_X]/mL
ATROPA BELLADONNA6 [hp_X]/mL
SALIX NIGRA BARK3 [hp_X]/mL
SUS SCROFA CEREBELLUM6 [hp_X]/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiU0NQ8555JD, WQZ3G9PF0H, QU52J3A5B3, 49NGK53TPQ

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83027-0087-1Facial Pain Formula60 mL in 1 BOTTLE, SPRAYSPRAY601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83027-0087FACIAL PAIN FORMULA (SALIX NIGRA, BELLADONNA, CEREBELLUM (SUIS), ACONITUM NAPELLUS) SPRAY [NUTRITIONAL SPECIALTIES, INC.]1Current NDC, 1 package rows20230707_e9281311-8ba8-4a5a-91a2-8a6bec0da0ad.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
83027-0087-18302700870160 mL in 1 BOTTLE, SPRAY (83027-0087-1) 60 ml2023-07-06NoNoCurrent