Medication Guide App

THE FLOWER UV INTENSE PACT SPF50 PA NB21

Dosage form: powder
Ingredients: ZINC OXIDE 1.64g in 12g, TITANIUM DIOXIDE 1.53g in 12g
Labeler: THEFACESHOP CO., LTD.
NDC Code: 51523-023

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Facts

Active Ingredients: TITANIUM DIOXIDE, ZINC OXIDE

Inactive Ingredients:

MICA(CI 77019), TALC, METHYL METHACRYLATE CROSSPOLYMER, ETHYLHEXYL METHOXYCINNAMATE, BORON NITRIDE, PHENYL TRIMETHICONE, DIMETHICONE, SILICA,
ETHYLHEXYL PALMITATE, IRON OXIDES(CI 77492), TRIETHOXYCAPRYLYLSILANE, METHICONE, CAPRYLIC / CAPRIC TRIGLYCERIDE, METHYLPARABEN, FRAGRANCE, IRON OXIDES(CI 77491), HYDROGENATED LECITHIN, BUTYLPARABEN, IRON OXIDES(CI 77499), ROSA CANINA FLOWER, JASMINUM OFFICINALE (JASMINE) FLOWER, ANTHEMIS NOBILIS FLOWER POWDER, PHALAENOPSIS AMABILIS EXTRACT, DENDROBIUM PHALAENOPSIS FLOWER EXTRACT, CAMELLIA JAPONICA FLOWER EXTRACT, LILIUM CANDIDUM BULB EXTRACT, IMPATIENS BALSAMINA FLOWER EXTRACT, PELARGONIUM GRAVEOLENS EXTRACT, CALENDULA OFFICINALIS FLOWER EXTRACT, HIBISCUS ROSA-SINENSIS FLOWER/LEAF EXTRACT, TROPAEOLUM MAJUS FLOWER/LEAF/STEM EXTRACT

Warnings:
When using this product
Keep out of eyes. Rinse with water to remove.
Stop use and ask a doctor if
Rash or irritation develops and lasts.

Directions:
Apply evenly before sun exposure and as needed.

THE FLOWER UV INTENSE PACT  SPF50 PA NB21
zinc oxide powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51523-023
Route of AdministrationCUTANEOUSDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (ZINC CATION) ZINC OXIDE1.64 g  in 12 g
TITANIUM DIOXIDE (TITANIUM) TITANIUM DIOXIDE1.53 g  in 12 g
Packaging
#Item CodePackage Description
1NDC:51523-023-0112 g in 1 CARTON
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35203/01/2007
Labeler - THEFACESHOP CO., LTD. (688329416)

Revised: 07/2010
 
THEFACESHOP CO., LTD.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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