FDA.reportPublic FDA data

STUBBLE and STACHE Broad Spectrum SPF 30

Manufacturer
Stubble & Stache LLC.
Effective date
2018-10-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:49:22

Label at a glance#

ProductSTUBBLE and STACHE Broad Spectrum SPF 30
Active ingredientOCTINOXATE, OCTISALATE, AVOBENZONE
Label structure8 sections

Dosage and administration

Apply liberally 15-minutes before sun exposure. Reapply: Immediately after swimming, sweating or towel drying. At least every 2 hours. Sun Protection Measure: Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF rating of 15 or higher, along with other sun protection measures including: Limit time in the sun, es...

Label contents#

Full prescribing information#

Active Ingredient:

OTC - ACTIVE INGREDIENT SECTION

Octinoxate 7.5%, Octisalate 5.0%,
Avobenzone 3.0%

Purpose:

OTC - PURPOSE SECTION

Sunscreen

Indications:

INDICATIONS & USAGE SECTION

  • Helps prevent Sunburn
  • If used as directed with other sun protection measures (see directions), decreases the risk of skin cancer and early skin aging caused by the sun.

Warnings:

WARNINGS SECTION

  • For external use only.

Do not use

OTC - DO NOT USE SECTION

on damaged or broken skin.

When using this product

OTC - WHEN USING SECTION

keep out of eyes. Rinse with water to remove.

Stop use and consult physician

OTC - STOP USE SECTION

if irritation or rash develops.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If product is swallowed, get medical attention or contact poison control center immediately.

Directions:

DOSAGE & ADMINISTRATION SECTION

  • Apply liberally 15-minutes before sun exposure.
  • Reapply:
  • Immediately after swimming, sweating or towel drying.
  • At least every 2 hours.
  • Sun Protection Measure: Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF rating of 15 or higher, along with other sun protection measures including:
  • Limit time in the sun, especially from 10 am to 2 pm.
  • Wear long-sleeved shirts, pants, hats, and sunglasses.
  • For children under 6-months, consult a physician.

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Argania Spinosa (Argan) Oil, Ascorbyl Palmitate (Vitamin C), Camellia Sinensis (Green Tea) Extract, Caprylic/Capric Triglyceride, Carbomer, Cetyl Alcohol, Cetearyl Olivate, Citric Acid, Cocos Nucifera (Coconut) Oil, Cucumis Sativus (Cucumber) Extract, Dimethicone, Ethylhexylglycerin, Eucalyptus Globulus Oil, Glycerin, Glyceryl Stearate, Glycyrrhiza Glabra (Licorice) Extract, Helianthus Annuus (Sunflower) Oil, Hyaluronic Acid, Lavandula Angustifolia (Lavender) Oil, Phenoxyethanol, Polysorbate-20, Saccharide Isomerate, Santalum Spicatum (Sandalwood) Oil, Simmondsia Chinensis (Jojoba) Oil, Sorbitan Olivate, Stearyl Alcohol, Tocopheryl Acetate (Vitamin E), Zemea (Corn) Propanediol.

Other information:

SPL UNCLASSIFIED SECTION

  • Protect this product from excessive heat and direct sun.

Questions or Comments:

OTC - QUESTIONS SECTION

Email us at: support@stubbleandstache.com

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

Products#

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

DailyMed product names page 1 of 1 · 33 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72588-93072588-930-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 31 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
ARGAN OIL4V59G5UW9XIACT
ASCORBYL PALMITATEQN83US2B0NIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
CARBOXYPOLYMETHYLENE0A5MM307FCIACT
CETYL ALCOHOL936JST6JCNIACT
CETEARYL OLIVATE58B69Q84JOIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
COCONUT OILQ9L0O73W7LIACT
CUCUMBERYY7C30VXJTIACT
DIMETHICONE92RU3N3Y1OIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
EUCALYPTUS OIL2R04ONI662IACT
GLYCERINPDC6A3C0OXIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
GLYCYRRHIZA GLABRA2788Z9758HIACT
HYALURONIC ACIDS270N0TRQYIACT
LAVENDER OILZBP1YXW0H8IACT
PHENOXYETHANOLHIE492ZZ3TIACT
POLYSORBATE 207T1F30V5YHIACT
SACCHARIDE ISOMERATEW8K377W98IIACT
SANTALUM SPICATUM OILH9LVS6REV4IACT
JOJOBA OIL724GKU717MIACT
SORBITAN OLIVATEMDL271E3GRIACT
STEARYL ALCOHOL2KR89I4H1YIACT
CORN0N8672707OIACT
OCTINOXATE4Y5P7MUD51ACTIB
OCTISALATE4X49Y0596WACTIB
AVOBENZONEG63QQF2NOXACTIB

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
074bb79b-c6e3-2430-e063-6294a90af6f63ef8ba3e-1aba-4afe-9081-59ca52e523e72023-10-09WarningsExact identifier
spl set id: 3ef8ba3e-1aba-4afe-9081-59ca52e523e7

Reported adverse events (FAERS/openFDA)#

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