Drug labels

Centella Calming SUNSCREEN

CENTELLA CALMING SUNSCREEN · GUANGZHOU YUSONG FINE CHEMICLS Co., Ltd · CUTANEOUS

HUMAN OTC DRUG
Open FDA's page for this record
Set ID
2dc0ee9b-d58b-fe40-e063-6394a90af439
ID
2dc0eea5-98b2-d312-e063-6294a90ab0e1
Effective time
20250209
Version
1
SPL product data elements

Centella Calming SUNSCREEN Centella Calming SUNSCREEN ALUMINUM HYDROXIDE SORBITAN SESQUIOLEATE PROPANEDIOL PEG-9 DIGLYCIDYL ETHER/SODIUM HYALURONATE CROSSPOLYMER XANTHAN GUM SODIUM HYALURONATE CAPRYLHYDROXAMIC ACID SODIUM S-(2-HYDROXY-3-(3-(TRIHYDROXYSILYL)PROPOXY)PROPYL) SULFUROTHIOATE TRIETHOXYCAPRYLYLSILANE ALPHA-TOCOPHEROL ACETATE LACTIC ACID CENTELLA ASIATICA TRITERPENOIDS HYDROLYZED CASEIN (ENZYMATIC; 1000 MW) SODIUM ACETYLATED HYALURONATE HYALURONIC ACID TITANIUM DIOXIDE TITANIUM DIOXIDE ETHYLHEXYL SALICYLATE ETHYLHEXYL SALICYLATE PHENYLBENZIMIDAZOLE SULFONIC ACID PHENYLBENZIMIDAZOLE SULFONIC ACID AQUA GLYCERIN SILICA BUTYLENE GLYCOL NEOPENTYL GLYCOL DIHEPTANOATE CYCLOPENTASILOXANE ISOHEXADECANE CETYL PEG/PPG-10/1 DIMETHICONE (HLB 4) C12-15 ALKYL BENZOATE CYCLOHEXASILOXANE NIACINAMIDE MAGNESIUM SULFATE DISTEARDIMONIUM HECTORITE MADECASSOSIDE 1,2-HEXANEDIOL PEG-10 DIMETHICONE (200 CST) ZINC OXIDE ZINC OXIDE HYDROXYACETOPHENONE SODIUM HYDROXIDE

Active ingredient
Active Ingredient(s) Zinc Oxide 2.85% Titanium Dioxide 2.76% EthylhexyI Salicylate 5% Phenylbenzimidazole Sulfonic Acid 3.2%
Purpose
Purpose Sunscreen
Indications and usage

Use ● Helps prevent sunburn. ● Ifused 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 For external use only
Do not use
Do not use Do not use on damaged or broken skin
When using
When using this product keep out of eyes. Rinse with water to remove
Stop use
Stop use and ask a doctor if rash occurs
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
Dosage and administration

Directions ●Apply liberally 15 minutes before sun exposure. ●Children under 6 months of age : Ask a doctor. ●Reapply at least every 2 hours, and after 40 minutes of swimming or sweating. ●Sun Protection Measures. 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 of 15 or higher and other sun protection measures including: ●limit time in the sun, especially from10 a.m.-2 p.m. ●wear long-sleeve shirts, pants, hats, and sunglasses

Storage and handling

Other information ●Protect the product in this container from excessive heat and direct sun. ●Sun alert : Limiting sun exposure, wearing protective clothing, and using sunscreens may reduce the risks of skin aging, skin cancer, and other harmful effects of the sun.

Inactive ingredient

Inactive ingredients Aqua, Glycerin, Silica, Butylene Glycol, Neopenty|l Gly-col Diheptanoate, Cyclopentasiloxane, Isohexadecane, Cety| Peg/Ppg-10/1 Dimethicone, C12-15 AlkyI Benzo-ate, Cyclohexasiloxane, Niacinamide, Magnesium Sul- fate, Disteardimonium Hectorite, Madecassoside,1,2-Hexanediol, Peg-10 Dimethicone, Sorbitan Sesqui- oleate, Hydroxyacetophenone, Sodium Hydroxide,

Package label principal display panel
Package Label - Principal Display Panel undefined
Harmonized identifiers (openFDA)
Application number
M020
Brand name
Centella Calming SUNSCREEN
Generic name
CENTELLA CALMING SUNSCREEN
Manufacturer name
GUANGZHOU YUSONG FINE CHEMICLS Co., Ltd
Product NDC
84558-007
Product type
HUMAN OTC DRUG
Route
CUTANEOUS
Substance name
TITANIUM DIOXIDE, ETHYLHEXYL SALICYLATE, PHENYLBENZIMIDAZOLE SULFONIC ACID, ZINC OXIDE
SPL ID
2dc0eea5-98b2-d312-e063-6294a90ab0e1
SPL set ID
2dc0ee9b-d58b-fe40-e063-6394a90af439
Package NDC
84558-007-01
Is original packager
true
UNII
15FIX9V2JP, 4X49Y0596W, 9YQ9DI1W42, SOI2LOH54Z
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.