Glow Go Lip Oil

Manufacturer
Northwest Cosmetic Laboratories LLC, DBA Elevation Labs, Idaho
Effective date
2024-03-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:07:14

Label at a glance#

ProductGlow Go Lip Oil
Active ingredientHOMOSALATE, OCTISALATE, OCTOCRYLENE, AVOBENZONE
Label structure13 sections

Dosage and administration

- Apply 20 minutes before sun exposure - Use a water resistant sunscreen if swimming or sweating - Re-apply frequently especially after swimming excercising or towel drying - Re-apply at least every 2 hours - Children under 6 months of age- ask a doctor

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

AVOBENZONE 3 %

HOMOSALATE 10%

OCTISALATE 5 %

OCTOCRYLENE 10%

PURPOSE

OTC - PURPOSE SECTION

SUNSCREEN

USE

INDICATIONS & USAGE SECTION

- Helps prevents sunburn

- If used as directed with other sun protection measures ( see directions) decreases the risk of skin cancer and early skin ageing caused by the sun.

WARNINGS

WARNINGS SECTION

FOR EXTERNAL USE ONLY

- Do not use on damaged or broken skin.

OTC - WHEN USING SECTION

keep out of eyes, Rinse with water to remove

Stop use & ask doctor

OTC - STOP USE SECTION

If rash occurs

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If product is swallowed , get medical help or contact a poison control center right away

Directions

INSTRUCTIONS FOR USE SECTION

- Apply 20 minutes before sun exposure

- Use a water resistant sunscreen if swimming or sweating

- Re-apply frequently especially after swimming excercising or towel drying

- Re-apply at least every 2 hours

- Children under 6 months of age- ask a doctor

Sun Protection Measures :

SUMMARY OF SAFETY AND EFFECTIVENESS

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 value of 15 or higher and other sun protection measures inclusing:

- limit time in the sun, especially from 10:00 AM- 02:00 PM

- Wear long- Sleeved shirts , pants, Hats and sunglasses

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Candelilla wax, Citrullus Lanatus Seed oil, Flavor, Isopropyl myristate, MICA, Octyldodecanol, Phenoxyethanol, Polybutene, Simmondsis Chinensis (jojoba) seed oil, Solanum Lycopersicum (Tomato) fruit extract,

OTHER SAFETY INFORMATION

Protect the product in this container from excessive heat & direct sun

DOSAGE & ADMINISTRATION SECTION

- Apply 20 minutes before sun exposure

- Use a water resistant sunscreen if swimming or sweating

- Re-apply frequently especially after swimming excercising or towel drying

- Re-apply at least every 2 hours

- Children under 6 months of age- ask a doctor

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62282-60062282-600-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 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
14a94d55-e11f-9a99-e063-6294a90a65f114a94d55-e11e-9a99-e063-6294a90a65f12024-03-27WarningsExact identifier
spl id: 14a94d55-e11f-9a99-e063-6294a90a65f1
spl set id: 14a94d55-e11e-9a99-e063-6294a90a65f1

Reported adverse events (FAERS/openFDA)#

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