FDA Label for Advanced Protection Sunscreen Spf-30

View Indications, Usage & Precautions

Advanced Protection Sunscreen Spf-30 Product Label

The following document was submitted to the FDA by the labeler of this product Botanical Science, Inc.. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.

Active Ingredients



ZINC OXIDE 7.0%

OCTINOXATE 7.5%

OCTISALATE 5.0%


Purpose



SUNSCREEN


Uses



HELPS PREVENT SUNBURN.


Warnings



FOR EXTERNAL USE ONLY.

  • AVOID CONTACT WITH EYES
  • DISCONTINUE USE IF SIGNS OF IRRITATION OR RASH APPEAR
  • STOP USE AND CONSULT A DOCTOR IF IRRITATION OR RASH PERSISTS

Directions



APPLY TO AREAS EXPOSED TO THE SUN. REAPPLY FREQUENTLY, ESPECIALLY AFTER PHYSICAL ACTIVITY OR SWIMMING.

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 Ingredients



AQUA, C12-15 ALKYL BENZOATE, GLYCERYL STEARATE, CETYL ALCOHOL, CETEARYL ETHYLHEXYLNOATE, CCYCLOPENTASILOXANE, CETARYL ALCOHOL, CETYL DIMETHICONE, ASCORBIC ACID, TOCOPHERYL ACETATE, CALENDULA OFFICINALIS FLOWER EXTRACT, CHAMOMILLA RECUTITA (MATRICARIA) FLOWER EXTRACT, GINKGO BILOBA LEAF EXTRACT, PEG-100 STEARATE, PANAX GINSENG ROOT EXTRACT, CAMELIA OLEIFERA LEAF EXTRACT, GLYCYRRHIZA GLABRA (LICORICE) ROOT EXTRACT, SODIUM PCA, SODIUM HYALURONATE, XANTHAN GUM, DEHYDROACETIC ACID, TRIETHOXYCAPRYLYLSILANE, BENZYL ALCOHOL, TETRASODIUM EDTA, CITRIC ACID.


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