COTTONSEED OIL - Aidance Skincare & Topical Solutions, LLC

Manufacturer: Aidance Skincare & Topical Solutions, LLC
Effective date: 2023-05-10
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: legacy-cache
Hydrated at: 2026-08-01 21:31:32

Label at a glance#

ProductTerragen HG Treatment Maximum Strength

Active ingredientGRAPHITE, RANUNCULUS BULBOSUS, SODIUM CHLORIDE, THUJA OCCIDENTALIS LEAFY TWIG

Label structure7 sections

Indications and uses

For the treatment of symptoms of herpes

Dosage and administration

Adults and children 12 years or over: Wash hands before and after applying Terragen. Apply to affected area at the first sign of an outbreak or tingling sensation. Early treatment ensures the best results. Rub in gently but completely. Do not use more than 3 times a day. Children under 12 years: ask a doctor. Store at room temperature.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Graphites, Natrum Muriaticum, Ranunculus Bulbosus, Thuja Occidentalis

The letters HPUS indicate the component(s) in this product is (are) officially monographed in the Homeopathic Pharmacopeia of the United States

Purpose

OTC - PURPOSE SECTION

Graphites - Relief for skin erruptions in genital area

Natrum Muriaticum - Blisters, itching and burning relief

Ranunculus Bulbosus - Herpes blisters, stinging pain relief

Thuja Occidentalis - Herpes, skin erruptions, burning pain relief

Uses

INDICATIONS & USAGE SECTION

For the treatment of symptoms of herpes

Warnings

WARNINGS SECTION

For external use only.
Virally based infections are contagious. This product will not stop the spread of the herpes virus or other viruses.
Do not use - in the eyes - over large areas of the body - if you are allergic to any ingredient in this product.
Ask a doctor before use if pregnant or nursing.
Stop use and ask a doctor if condition worsens or symptoms persist for more than 7 days.

Directions

DOSAGE & ADMINISTRATION SECTION

Inactive Ingredients

INACTIVE INGREDIENT SECTION

beeswax (organic), cotton seed oil, cedarwood oil, jojoba seed oil, magnesium oxide, silver oxide, stearic acid (naturally sourced), zinc oxide.

PRINCIPAL DISPLAY PANEL - 14g Tube

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

terragen™
HG FORMULA MAX

HG Treatment

Terragen

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
GRAPHITE	ACTIVE INGREDIENT	4QQN74LH4O	1
RANUNCULUS BULBOSUS	ACTIVE INGREDIENT	AEQ8NXJ0MB	1
SODIUM CHLORIDE	ACTIVE INGREDIENT	451W47IQ8X	1
THUJA OCCIDENTALIS LEAFY TWIG	ACTIVE INGREDIENT	1NT28V9397	1
GRAPHITE	ACTIVE MOIETY	4QQN74LH4O	1
RANUNCULUS BULBOSUS	ACTIVE MOIETY	AEQ8NXJ0MB	1
SODIUM CATION	ACTIVE MOIETY	LYR4M0NH37	1
THUJA OCCIDENTALIS LEAFY TWIG	ACTIVE MOIETY	1NT28V9397	1
JOJOBA OIL	INACTIVE INGREDIENT	724GKU717M	1
JUNIPERUS VIRGINIANA OIL	INACTIVE INGREDIENT	PAD4FN7P2G	1
MAGNESIUM OXIDE	INACTIVE INGREDIENT	3A3U0GI71G	1
SILVER OXIDE	INACTIVE INGREDIENT	897WUN6G6T	1
WHITE WAX	INACTIVE INGREDIENT	7G1J5DA97F	1
ZINC OXIDE	INACTIVE INGREDIENT	SOI2LOH54Z	1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

Terragen HG Treatment Maximum Strength
Graphites, Natrum Muriaticum, Ranunculus Bulbosus, Thuja Occidentalis
COTTONSEED OIL
JOJOBA OIL
JUNIPERUS VIRGINIANA OIL
MAGNESIUM OXIDE
SILVER STEARATE
WHITE WAX
ZINC OXIDE
GRAPHITE
RANUNCULUS BULBOSUS
SODIUM CHLORIDE
SODIUM CATION
THUJA OCCIDENTALIS LEAFY TWIG

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
24909-143	24909-143-14, 24909-143-15, 24909-143-44, 24909-143-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
COTTONSEED OIL	H3E878020N	IACT
JOJOBA OIL	724GKU717M	IACT
JUNIPERUS VIRGINIANA OIL	PAD4FN7P2G	IACT
MAGNESIUM OXIDE	3A3U0GI71G	IACT
SILVER STEARATE	4H6PCL92ZN	IACT
WHITE WAX	7G1J5DA97F	IACT
ZINC OXIDE	SOI2LOH54Z	IACT
GRAPHITE	4QQN74LH4O	ACTIB
RANUNCULUS BULBOSUS	AEQ8NXJ0MB	ACTIB
SODIUM CHLORIDE	451W47IQ8X	ACTIB
THUJA OCCIDENTALIS LEAFY TWIG	1NT28V9397	ACTIB

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 30 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
WHITE WAX	WHITE WAX	7G1J5DA97F	TABLET, DELAYED RELEASE / ORAL	0.08 mg		Exact identifier — unii candidate 15 equally ranked IID candidates
WHITE WAX	WHITE WAX	7G1J5DA97F	TABLET / ORAL	5 mg		Exact identifier — unii candidate 15 equally ranked IID candidates
ZINC OXIDE	ZINC OXIDE	SOI2LOH54Z	LOTION / TOPICAL	16 %w/w		Exact identifier — unii candidate 6 equally ranked IID candidates
ZINC OXIDE	ZINC OXIDE	SOI2LOH54Z	INJECTION, SUSPENSION / SUBCUTANEOUS	NA		Exact identifier — unii candidate 6 equally ranked IID candidates
WHITE WAX	WHITE WAX	7G1J5DA97F	TABLET, FILM COATED / ORAL	0.2 mg		Exact identifier — unii candidate 15 equally ranked IID candidates
MAGNESIUM OXIDE	MAGNESIUM OXIDE	3A3U0GI71G	TABLET, DELAYED RELEASE / ORAL		368 mg	Exact identifier — unii candidate 9 equally ranked IID candidates
WHITE WAX	WHITE WAX	7G1J5DA97F	LOTION / TOPICAL	1 %w/w		Exact identifier — unii candidate 15 equally ranked IID candidates
WHITE WAX	WHITE WAX	7G1J5DA97F	CREAM / TOPICAL		500 mg	Exact identifier — unii candidate 15 equally ranked IID candidates
MAGNESIUM OXIDE	MAGNESIUM OXIDE	3A3U0GI71G	CAPSULE, EXTENDED RELEASE / ORAL		75 mg	Exact identifier — unii candidate 9 equally ranked IID candidates
WHITE WAX	WHITE WAX	7G1J5DA97F	CAPSULE, EXTENDED RELEASE / ORAL		71 mg	Exact identifier — unii candidate 15 equally ranked IID candidates
MAGNESIUM OXIDE	MAGNESIUM OXIDE	3A3U0GI71G	TABLET, FILM COATED / ORAL		80 mg	Exact identifier — unii candidate 9 equally ranked IID candidates
MAGNESIUM OXIDE	MAGNESIUM OXIDE	3A3U0GI71G	CAPSULE / ORAL		20 mg	Exact identifier — unii candidate 9 equally ranked IID candidates
WHITE WAX	WHITE WAX	7G1J5DA97F	TABLET, COATED / ORAL	3 mg		Exact identifier — unii candidate 15 equally ranked IID candidates
MAGNESIUM OXIDE	MAGNESIUM OXIDE	3A3U0GI71G	CAPSULE, DELAYED RELEASE / ORAL		78 mg	Exact identifier — unii candidate 9 equally ranked IID candidates
ZINC OXIDE	ZINC OXIDE	SOI2LOH54Z	INJECTION / SUBCUTANEOUS	0.02 %w/v		Exact identifier — unii candidate 6 equally ranked IID candidates
MAGNESIUM OXIDE	MAGNESIUM OXIDE	3A3U0GI71G	TABLET, EXTENDED RELEASE / ORAL	25.74 mg		Exact identifier — unii candidate 9 equally ranked IID candidates
WHITE WAX	WHITE WAX	7G1J5DA97F	OINTMENT, AUGMENTED / TOPICAL		429 mg	Exact identifier — unii candidate 15 equally ranked IID candidates
WHITE WAX	WHITE WAX	7G1J5DA97F	CREAM / VAGINAL		40 mg	Exact identifier — unii candidate 15 equally ranked IID candidates
WHITE WAX	WHITE WAX	7G1J5DA97F	AEROSOL, FOAM / TOPICAL	2 %w/w		Exact identifier — unii candidate 15 equally ranked IID candidates
ZINC OXIDE	ZINC OXIDE	SOI2LOH54Z	SUPPOSITORY / RECTAL	375 mg		Exact identifier — unii candidate 6 equally ranked IID candidates
ZINC OXIDE	ZINC OXIDE	SOI2LOH54Z	SOLUTION / RESPIRATORY (INHALATION)	3.11 %w/v		Exact identifier — unii candidate 6 equally ranked IID candidates
MAGNESIUM OXIDE	MAGNESIUM OXIDE	3A3U0GI71G	TABLET / SUBLINGUAL		15 mg	Exact identifier — unii candidate 9 equally ranked IID candidates
MAGNESIUM OXIDE	MAGNESIUM OXIDE	3A3U0GI71G	TABLET / ORAL		63 mg	Exact identifier — unii candidate 9 equally ranked IID candidates
WHITE WAX	WHITE WAX	7G1J5DA97F	CAPSULE / ORAL		79 mg	Exact identifier — unii candidate 15 equally ranked IID candidates
MAGNESIUM OXIDE	MAGNESIUM OXIDE	3A3U0GI71G	GUM, CHEWING / BUCCAL		173 mg	Exact identifier — unii candidate 9 equally ranked IID candidates
WHITE WAX	WHITE WAX	7G1J5DA97F	OINTMENT / TOPICAL		2100 mg	Exact identifier — unii candidate 15 equally ranked IID candidates
ZINC OXIDE	ZINC OXIDE	SOI2LOH54Z	SOLUTION / INTRAVENOUS	3.11 %w/v		Exact identifier — unii candidate 6 equally ranked IID candidates
WHITE WAX	WHITE WAX	7G1J5DA97F	CREAM, AUGMENTED / TOPICAL	10 %w/w		Exact identifier — unii candidate 15 equally ranked IID candidates
WHITE WAX	WHITE WAX	7G1J5DA97F	TABLET, EXTENDED RELEASE / ORAL	14 mg		Exact identifier — unii candidate 15 equally ranked IID candidates
WHITE WAX	WHITE WAX	7G1J5DA97F	SUPPOSITORY / RECTAL	265 mg		Exact identifier — unii candidate 15 equally ranked IID candidates

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
193cae2c-be99-5302-e063-6294a90adaaf			c8b3d0df-1db5-4c12-ae54-acdd19732fb0	2024-05-24	Warnings	Exact identifier spl set id: c8b3d0df-1db5-4c12-ae54-acdd19732fb0

Reported adverse events (FAERS/openFDA)#

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