Beeswax SPF 15 Broad Spectrum Lip Balm
BEESWAX SPF 15 BROAD SPECTRUM LIP BALM · Raining Rose, Inc · TOPICAL
Open FDA's page for this record- Set ID
- 2dcc2f9b-4a8c-b281-e063-6294a90ad9d6
- ID
- 2dcc2d3b-8a0f-19f3-e063-6394a90ad455
- Effective time
- 20250210
- Version
- 5
- SPL product data elements
Beeswax SPF 15 Broad Spectrum Lip Balm Beeswax SPF 15 Broad Spectrum Lip Balm SUNFLOWER OIL MONO/DIGLYCERIDES CANOLA OIL SOYBEAN OIL WHITE WAX SUNFLOWER OIL TOCOPHEROL ROSEMARY OLIVE OIL CANNABIS SATIVA SEED OIL ALOE VERA LEAF OCTISALATE OCTISALATE AVOBENZONE AVOBENZONE OCTOCRYLENE OCTOCRYLENE OCTINOXATE OCTINOXATE
- Active ingredient
- Active Ingredients Avobenzone 2.0% Octinoxate 6.5% Octisalate 5.0% Octocrylene 1.5%
- Purpose
- Purpose Sunscreen
- Warnings
- Warnings For external use only
- Do not use
- Do not use on damaged or broken skin.
- Stop use
- Stop Use and ask a doctor if Rash Occurs
- When using
- When Using this Product Keep out of eyes. Rinse well with water to remove.
- Keep out of reach of children
- Keep out of reach of children Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
- Route
Directions Apply liberally 15 minutes before sun exposure Use a water resistant sunscreen if swimming or sweating Reapply at least every 2 hours Children under 6 months of age: Ask a doctor
- Inactive ingredient
Inactive ingredients: Sunflower Oil*, Beeswax, Olive Oil*, Tocopherol, Hemp Seed Oil*, Rosemary Extract, Aloe Extract, Soybean Oil, Canola Oil, Sunflower Seed Oil Glycerides. * Organic
- Dosage and administration
- Apply liberally 15 mintues before sun exposure
- Indications and usage
- Helps prevent sunburn
- Package label principal display panel
- Package Label C10401 BEESWAX PREMIUM SPF 15 BS LB
- Harmonized identifiers (openFDA)
- Application number
- M020
- Brand name
- Beeswax SPF 15 Broad Spectrum Lip Balm
- Generic name
- BEESWAX SPF 15 BROAD SPECTRUM LIP BALM
- Manufacturer name
- Raining Rose, Inc
- Product NDC
- 65692-0591
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Substance name
- OCTISALATE, AVOBENZONE, OCTOCRYLENE, OCTINOXATE
- SPL ID
- 2dcc2d3b-8a0f-19f3-e063-6394a90ad455
- SPL set ID
- 2dcc2f9b-4a8c-b281-e063-6294a90ad9d6
- Package NDC
- 65692-0591-1
- Is original packager
- true
- UNII
- 4X49Y0596W, G63QQF2NOX, 5A68WGF6WM, 4Y5P7MUD51