Doc Block Daily Sunscreen Broad Spectrum SPF55: Package Insert and Label Information

DOC BLOCK DAILY SUNSCREEN BROAD SPECTRUM SPF55- octocrylene, homosalate, avobenzone and octisalate lotion
Garth Fisher Beauty LLC

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.

Active Ingredients

Avobenzone 3.0%

Homosalate 10.0%

Octisalate 5.0%

Octocrylene 7.0%

Purpose

Sunscreen

Uses

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 Poison Control right away.

Directions

– Apply liberally 15 minutes befor sun exposure.

– Use a water resistant sunscreen if swimming or sweating.

– Reapply at least every 2 hours.

– Children undert 6 months: ask a doctor.

– 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 value of 15 or higher.

– Limit time in the sun, especially from 10 a.m. — 2 p.m.

– Wear long-sleeve shirts, pants, hats, and sunglasses.

Inactive ingredients

Water, C12-15 Alkyl Benzoate, Cyclopentasiloxane, Hydrated Silica, Propane Diol, Cetearyl Alcohol, Dimethicone, Tocopheryl Acetate, Osmanthus Fragrans Flower Extract, Camellia Sinensis Leaf Extract, Butyrospermum Parkii (Shea) Butter Extract, Butyrospermum Parkii (Shea) Butter, Shorea Robusta Seed Butter, Elaesis Guineensis (Palm) Butter, Theobroma Cacao (Cocoa) Seed Butter, Bassia Latifolia Seed Butter, Mangifera Indica (Mango) Seed Butter, Garcinia Indica Seed Butter, Illipe Butter, Theobroma Grandiflorum Seed Butter, Astrocaryum Murumuru Seed Butter, Astrocaryum Tucuma Seed Butter, Phospholipids, Helianthus Annuus (Sunflower) Seed Oil, Allantoin, Sorbitol, Glycerin, Lecithin, Xanthan Gum, Oleic Acid, Phenoxyethanol, Ethylhexylglycerin, Glyceryl Stearate, PEG-100 Stearate, Carbomer, Aminomethyl Propanol, Potassium Cetyl Phosphate, Urea

Other Information

– Protect the product in this container from excessive heat and direct sun.

– May stain fabrics

Questions?

120 South Spaulding Drive, Suite 222,

Beverly Hills, CA 90212

Keep Out of Reach of Children

Keep out o reach of children. If product is swallowed get medical help or contact a Poison Control Center right away.

Label

Label
(click image for full-size original)

DOC BLOCK DAILY SUNSCREEN BROAD SPECTRUM SPF55
sunscreen lotion
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:71873-101
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
OCTOCRYLENE (OCTOCRYLENE) OCTOCRYLENE 7 g in 100 g
HOMOSALATE (HOMOSALATE) HOMOSALATE 10 g in 100 g
AVOBENZONE (AVOBENZONE) AVOBENZONE 3 g in 100 g
OCTISALATE (OCTISALATE) OCTISALATE 5 g in 100 g
Inactive Ingredients
Ingredient Name Strength
WATER
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:71873-101-11 1 TUBE in 1 CARTON contains a TUBE (71873-101-01)
1 NDC:71873-101-01 50 g in 1 TUBE This package is contained within the CARTON (71873-101-11)
2 NDC:71873-101-12 1 TUBE in 1 CARTON contains a TUBE (71873-101-02)
2 NDC:71873-101-02 7.4 g in 1 TUBE This package is contained within the CARTON (71873-101-12)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part352 06/08/2018
Labeler — Garth Fisher Beauty LLC (080828501)
Establishment
Name Address ID/FEI Operations
Garth Fisher Beauty LLC 080828501 label (71873-101)
Establishment
Name Address ID/FEI Operations
Quest 927768135 manufacture (71873-101)

Revised: 08/2018 Garth Fisher Beauty LLC

DrugInserts.com provides trustworthy package insert and label information about marketed drugs as submitted by manufacturers to the US Food and Drug Administration. Package information is not reviewed or updated separately by DrugInserts.com. Every individual package label entry contains a unique identifier which can be used to secure further details directly from the US National Institutes of Health and/or the FDA.

As the leading independent provider of trustworthy medication information, we source our database directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. Our material is not intended as a substitute for direct consultation with a qualified health professional.

Terms of Use | Copyright © 2021. All Rights Reserved.