Hair-Scalp

Manufacturer
Newton Laboratories, Inc.
Effective date
2019-10-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:48:07

Label at a glance#

ProductHair-Scalp
Active ingredientAPIS MELLIFERA, ARSENIC TRIOXIDE, OYSTER SHELL CALCIUM CARBONATE, CRUDE, SOLANUM DULCAMARA TOP, GRAPHITE, CALCIUM SULFIDE, GOLDENSEAL, HYDROFLUORIC ACID, POTASSIUM CARBONATE, LYCOPODIUM CLAVATUM SPORE, DAPHNE MEZEREUM BARK, NERIUM OLEANDER LEAF, KEROSENE, PHOSPHORIC ACID, PHOSPHORUS, TOXICODENDRON PUBESCENS LEAF, SELENIUM, SEPIA OFFICINALIS JUICE, SILICON DIOXIDE, SULFUR, THUJA OCCIDENTALIS LEAFY TWIG
Label structure10 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Formulated for associated symptoms such as dandruff, hair loss, premature graying, soreness and sensitivity.

DOSAGE & ADMINISTRATION SECTION

Directions: Ages 12 and up, take 6 pellets by mouth (ages 0 to 11, give 3 pellets) as needed or as directed by a health professional. Under age 2, crush/dissolve pellets in purified water. Sensitive persons begin with 1 pellet and gradually increase to full dose.

OTC - ACTIVE INGREDIENT SECTION

Equal parts of Hydrastis 6x, Thuja occ. 6x, Apis mel. 15x, Arsenicum alb. 15x, Calc.carb. 15x, Dulcamara 15x, Graphites 15x, Hepar sulph. calc. 15x, Hydrastis 15x, Hydrofluoricum ac. 15x, Kali carb. 15x, Lycopodium 15x, Mezereum 15x, Oleander 15x, Petroleum 15x, Phosphoricum ac. 15x, Phos. 15x, Rhus tox. 15x, Selenium 15x, Sepia 15x, Silicea 15x, Sulphur 15x.

OTC - PURPOSE SECTION

Formulated for associated symptoms such as dandruff, hair loss, premature graying, soreness and sensitivity.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Gluten-free, non-GMO, beet-derived sucrose (lactose-free) pellets.

QUESTIONS SECTION

OTC - QUESTIONS SECTION

newtonlabs.net - Questions? 800.448.7256

Newton Laboratories, Inc. FDA Est # 1051203 Conyers, GA 30013

WARNINGS SECTION

WARNINGS: Keep out of reach of children. Do not use if tamper-evident seal is broken or missing. If symptoms worsen or persist for more than a few days, consult a doctor. If pregnant or breast-feeding, ask a doctor before use.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a doctor before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

PACKAGE LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package labelpackage label

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55714-244955714-2449-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Source Document#

Source XML

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
9ab38f9e-2b49-519a-e053-2a95a90a49329ab39bde-ef00-51b8-e053-2a95a90ac3082019-10-15WarningsExact identifier
spl id: 9ab38f9e-2b49-519a-e053-2a95a90a4932
spl set id: 9ab39bde-ef00-51b8-e053-2a95a90ac308

Reported adverse events (FAERS/openFDA)#

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