Hand Goo

Manufacturer
Spry Life LLC
Effective date
2023-12-30
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 02:25:17

Label at a glance#

ProductHand Goo
Active ingredientACHILLEA MILLEFOLIUM FLOWER, ST. JOHN'S WORT, STELLARIA MEDIA, CALENDULA OFFICINALIS FLOWER, PLANTAGO MAJOR, COMMIPHORA MYRRHA WHOLE, SALVIA OFFICINALIS WHOLE, COMFREY LEAF
Label structure9 sections

Storage and handling

Store at room temperature.

Label contents#

Full prescribing information#

Purpose Section

OTC - PURPOSE SECTION

Skin Protectant

Astringent

External Analgesic

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Organic Calendula Officinalis (Calendula) Flower Oil 1X (HPUS)
Organic Plantago Major (Plantain) Leaf Extract 1X (HPUS)
Organic Stellaria Media (Chickweed) Extract 1X (HPUS)
Organic Symphytum Officinale (Comfrey) Leaf Powder 1X (HPUS)

OrganicAchilleaMillefolium(Yarrow)Extract1X(HPUS)

Commiphora Myrrha (Myrrh) Resin 1X (HPUS)

Organic Salvia Officinalis (Sage) Leaf 1X (HPUS)
Organic Hypericum Perforatum (St. John’s Wort) Oil 1X (HPUS).

Indications & Usage

INDICATIONS & USAGE SECTION

■ temporarily protects minor ■ cuts ■ scrapes ■ abrasions ■ blisters ■ burns
■ helps prevent and temporarily protects and helps relieve ■ chapped or cracked skin■ helps protect from the drying effects of wind and cold weather
■ temporarily protects and helps relieve minor skin irritation and itching due to

■ poison ivy ■ insect bites ■ rashes caused by soaps, detergents, cosmetics, or jewelry

■ temporarily protects and helps relieve minor pain associated with ■ calluses

■ blisters ■ abrasions ■ bruises ■ cuts ■ minor burns ■ scrapes

Keep out of reach of children section

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Warnings Section

Warnings

For external use only.

■ Do not use on ■ on deep wounds ■ animal bites ■ serious burns
■ Stop use and ask a doctor if ■ condition worsens ■ symptoms last more than 7 days or clear up and occur again within a few days

■ When using this product keep out of eyes. Rinse with water to remove.

Storage

STORAGE AND HANDLING SECTION

Store at room temperature.

Dosage & Administration Section

Apply as often as needed to affected area.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

OrganicOleaEuropaea(Olive)FruitOil,Organic Helianthus Annuus (Sunflower) Seed Oil, Organic Cera Alba (Beeswax), Styrax Benzoin Gum, Organic Larrea Tridentata (Chapparal) Extract, Tocopherol (Vitamin E), Lavandula Angustifolia (Lavender) Oil, Rosmarinus Officinalis (Rosemary) Leaf Oil.

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hand GooHand Goo

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70994-203-042025-01-30C16284748780-12cef2736-958e-d83d-e063-dadaa90ab31fHand Goo
70994-203-082025-01-30C16284748780-12cef2736-958e-d83d-e063-dadaa90ab31fHand Goo
70994-203-102025-01-30C16284748780-12cef2736-958e-d83d-e063-dadaa90ab31fHand Goo

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70994-203-02Hand Goo51.7 g in 1 CANSALVE51.76
70994-203-04Hand Goo17 g in 1 TUBESALVE176
70994-203-08Hand Goo113.4 g in 1 JARSALVE113.46
70994-203-10Hand Goo1 in 1 BOXSALVE16

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70994-203HAND GOO (CALENDULA OFFICIALS, STELLARIA MEDIA, ST. JOHNS WORT, ROSEMARY OIL, PLANTAGO MAJOR, COMMIPHORA MYRRHA, COMFREY LEAF, SALVIA OFFICINALIS, SUNFLOWER OIL) SALVE [SPRY LIFE LLC]6Legacy NDC, 4 package rows20231231_480e32e4-42df-606c-e054-00144ff8d46c.zip

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70994-20370994-203-04, 70994-203-02, 70994-203-10, 70994-203-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 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
0dbc5a3a-170f-d08f-e063-6294a90a50c6480e32e4-42df-606c-e054-00144ff8d46c2023-12-30WarningsExact identifier
spl id: 0dbc5a3a-170f-d08f-e063-6294a90a50c6
spl set id: 480e32e4-42df-606c-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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