Hair and Nail Tonic

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Hair and Nail Tonic
Generic name: AVENA, DNA, ELAEIS, GLANDULA SUPRARENALIS SUIS, HAMAMELIS, HEPAR SUIS, KALI SULPH, NAT MUR, NICOTINAMIDUM, PHOSPHORICUM AC, PITUITARUM POSTERIUM, RIBOFLAVINUM, THIAMINUM HYDROCHLORICUM, THUJA OCC, THYROIDINUM, URTICA UR.
Manufacturer: Eight and Company L.L.C
Product type: HUMAN OTC DRUG
SPL set ID: 35bda785-b3a7-4928-aaea-27bf9fb6abb5
SPL ID: 1513fb0c-15e7-4ba5-af36-3d032841f862
Version: 8
Effective date: 2025-12-18
Source export date: 2026-10-12
Source partition: 10
Source file: https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:29:05

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 24 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Hair and Nail Tonic	openfda.brand_name
generic name		AVENA, DNA, ELAEIS, GLANDULA SUPRARENALIS SUIS, HAMAMELIS, HEPAR SUIS, KALI SULPH, NAT MUR, NICOTINAMIDUM, PHOSPHORICUM AC, PITUITARUM POSTERIUM, RIBOFLAVINUM, THIAMINUM HYDROCHLORICUM, THUJA OCC, THYROIDINUM, URTICA UR.	openfda.generic_name
manufacturer name		Eight and Company L.L.C	openfda.manufacturer_name
ndc	package	61096-1022-1	openfda.package_ndc
ndc	product	61096-1022	openfda.product_ndc
ndc11	package	61096102201	derived:openfda.package_ndc
spl id		1513fb0c-15e7-4ba5-af36-3d032841f862	id
spl set id		35bda785-b3a7-4928-aaea-27bf9fb6abb5	set_id
unii		51FI676N6F	openfda.unii
unii		0B4FDL9I6P	openfda.unii
unii		25X51I8RD4	openfda.unii
unii		TLM2976OFR	openfda.unii
unii		80T6U6714J	openfda.unii
unii		1NT28V9397	openfda.unii
unii		451W47IQ8X	openfda.unii
unii		IHN2NQ5OF9	openfda.unii
unii		L0PFEMQ1DT	openfda.unii
unii		1K573LC5TV	openfda.unii
unii		M572600E5P	openfda.unii
unii		398IYQ16YV	openfda.unii
unii		MA9CQJ3F7F	openfda.unii
unii		E4GA8884NN	openfda.unii
unii		6EC706HI7F	openfda.unii
unii		T7S323PKJS	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS: If symptoms persist or worsen , stop use and seek advice of physician. If pregnant or breast-feeding, ask a health care professional before use. Keep out of reach of children. Contains alcohol, in case of overdose, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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