Quick answers
- What is Octinoxate and octocrylene used for?
- The Drug Facts label of Sunscreen Lip Protectionbroad Spectrum Spf 15 (Guangzhou Tata Biotechnology Co., Ltd.) lists these uses: protect lips from damaging UVA and UVB rays..
- Do I need a prescription for Octinoxate and octocrylene?
- No. The products on this page are sold without a prescription (over the counter).
- Is a store brand the same as the name brand?
- Products listed together below have the same active ingredients, in the same amount and the same form, as registered with the FDA. Inactive ingredients (such as colors, flavors and fillers) and package sizes can differ. Compare the “Active ingredient” box on both packages, and ask a pharmacist if you are not sure.
- Has Octinoxate and octocrylene been recalled?
- No recall linked to these products appears in the FDA enforcement reports we use.
Drug Facts label
Every over-the-counter medicine must carry a “Drug Facts” box in the same order, set by FDA rules. Below is the label of one product for each common strength and form, quoted word for word. Your own package can differ (for example, children’s products have other directions): always follow the label on your package.
Sunscreen Lip Protectionbroad Spectrum Spf 15 · Guangzhou Tata Biotechnology Co., Ltd.
Octinoxate 7.5 mg/100 mL · Octocrylene 5 mg/100 mL, gel (topical)
Active ingredient
Ethylhexyl Methoxycinnamate 7.5% Octocrylene 5%
Purpose
Sunscreen
Uses
protect lips from damaging UVA and UVB rays.
Warnings
For external use only.
Do not use
on damaged or broken skin
When using this product
keep out of eyes. Rinse with water to remove.
Stop use and ask a doctor if
rash occurs.
Keep out of reach of children
If product is swallowed, get medical help or contact a Poison Control Center right away.
Directions
Step 1:Saueeze tube. Step 2:Apply liberally and evenly to lips 15 to 20 minutes before exposure to the sun. Step3:Reapply after periods of swimming exercise and towel drying or as required.
Other information
Protect this product from excessive heat anddirect sun.
- Sun alert: Limiting sun exposure, wearing protective clothing,and using sunscreens may reduce the risk of skin aging, skin cancer,and other harmful effects of the sun.
Inactive ingredients
Ethylhexyl Palmitate, Polyisobutene,Petrolatum,Microcrystalline Wax,Hydrogenated Styrene/lsoprene Copolymer,PentaerythritylTetra-Di-T-ButylHydroxyhydrocinnamate,Beeswax, Synthetic Wax, Tocopheryl Acetate, Tridecyl Trimellitate,Simmondsia Chinensis (Jojoba) Seed Oil,Macadamia Integrifolia Seed Oil, Limnanthes Alba(Meadowfoam)Seed Oi,Butyrospermum Parkii (Shea) Butter, Hydrogenated Coconut Oil,Phenoxyethanol,Ethylhexylglycerin,Fragrance,FD&C YELLOW NO.5(C119140),TheobromaCacao(Cocoa)Extract, Dextrin,Phytosteryl/OctyldodecylLauroyl, Glutamate,Tocopherol
Questions?
You can email us at info@redi-usa.com for more help!
— FDA label of Sunscreen Lip Protectionbroad Spectrum Spf 15, Guangzhou Tata Biotechnology Co., Ltd., effective December 22, 2025. See the official label on DailyMed →
HEY HOTTIE Shimmer dry oil mist sunscreen spf30 · Guangdong Aimu Biological Technology Co., Ltd
Octinoxate 7.5% · Octocrylene 2%, spray (topical)
Active ingredient
OCTOCRYLENE 2 % OCTINOXATE 7.5%
Purpose
Sunscreen
Uses
Helps prevent sunburn. If used as directed with other sun protection measures (see Directions) decreases the risk ofskin cancer and early skin aging caused by the sun.
Warnings
For external use only. Do Not Use on damaged or broken skin.
When using this product
keep out of eyes. Rinse with water to remove.
Stop use and ask a doctor if
rash occurs. Keep Out Of Reach Of Children If swallowed, get medical help or contact a Poison Control Center right away.
Directions
*Shake well and spray directly onto skin evenly 15 minutes before sun exposure. *Reapply at least every 2 hours use a water resistant sunscreen if swimming or sweating. *Sun Protection Measures: Spending time in the sun increases your risk of skin cancer andearly skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPFvalue of 15 or higher and other sun protection measures including: -limit time in the sun, especially from 10 a.m. -2 p.m.wear long-sleeved shirts, pants, hats, and sunglasses. *Children under 6 months of age: Ask a doctor.
Inactive ingredients
ALCOHOL,SIMMONDSIACHINENSIS(JOJOBA)SEEDOIL,POLYMETHYLSILSESQUIOXANE,CYCLOPENTASILOXANE,PARFUM,BISABOLOL,CI 77491
— FDA label of HEY HOTTIE Shimmer dry oil mist sunscreen spf30, Guangdong Aimu Biological Technology Co., Ltd, effective June 10, 2026. See the official label on DailyMed →
This page is not medical advice. Read the label on your package, and ask a pharmacist or doctor if you are not sure a medicine is right for you, for your child, or with your other medicines.
Same medicine, other brands
Each group lists the products that have exactly the same active ingredients, in the same amount and form, as registered with the FDA (NDC Directory). A store brand in the same group has the same medicine as the name brand; inactive ingredients, flavors and package sizes can differ. Each product links to its own official label.
Octinoxate 7.5 mg/100 mL · Octocrylene 5 mg/100 mL · gel (topical) · 1 product
Drug Facts for this strength and form ↑
| Brand or product name | Company on the label | Label |
|---|---|---|
| Sunscreen Lip Protectionbroad Spectrum Spf 15 | Guangzhou Tata Biotechnology Co., Ltd. | DailyMed |
Octinoxate 7.5% · Octocrylene 2% · spray (topical) · 1 product
Drug Facts for this strength and form ↑
| Brand or product name | Company on the label | Label |
|---|---|---|
| HEY HOTTIE Shimmer dry oil mist sunscreen spf30 | Guangdong Aimu Biological Technology Co., Ltd | DailyMed |
Companies that sell this medicine
The company named on the package (maker or distributor), as listed in the FDA NDC Directory, with its number of over-the-counter products of this medicine.
- Guangzhou Tata Biotechnology Co., Ltd.1 product
- Guangdong Aimu Biological Technology Co., Ltd1 product
Recalls
No recall linked to these products (by their NDC code or label) appears in the FDA enforcement reports.
Sources
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- FDA rule for the Drug Facts label (21 CFR 201.66)
Only medicines marketed under FDA rules for nonprescription drugs (an FDA monograph or an FDA approval) are listed. Homeopathic products are not listed: the FDA does not evaluate them for safety or effectiveness.