OTC Medication Information: Japanese Cherry Blossom

JAPANESE CHERRY BLOSSOM- alcohol gel
Brands International Corp

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.

Ethyl Alcohol 62%

Purpose — Antiseptic

Use

  • To decrease bacteria on the skin and clean hands
  • recommened for repeated use

Warnings

For external use only

Flammable, Keep away from fire or flame

Keep out of children

If accidently swallowed, get medical help or contact a Poison Control Center right away

Do not get into eyes

If contact occurs, rinse thoroughly with water

Discontinue use if irritation or redness develop. If irritation persists for more than 72 hrs, consult a doctor

Directions

  • apply to hands until thoroughly wet
  • rub vigorously unti dry
  • supervise children in the use of this product

Other Information

  • May discolor certain fabrics or surfaces
  • do not store above 110 F ( 43 C)

Water, Isopropyl Alcohol, Glycerin, Carbomer, Aminomethyl Propanol, Fragrance, Proylene glycol, Isopropyl Myristate, Aloe Barbadensis Leaf Juice, Tocopheryl (Vitamin E) Actetate, Sunflower (Helianthus Annuus) Seed Extract, Grapefruit (Citrus Grandis), Seed Extract, Red 40 (Cl 16035), Red 33 (Cl 17200)

Japanese Cherry Blossom Antibacterial Hand Sanitizer Gel
(click image for full-size original)

JAPANESE CHERRY BLOSSOM
antibacterial hand sanitizer gel gel
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:50157-115
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALCOHOL (ALCOHOL) ALCOHOL 620 mL in 1000 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN
CARBOMER 940
AMINOMETHYLPROPANOL
PROPYLENE GLYCOL
.ALPHA.-TOCOPHEROL ACETATE
FD&C RED NO. 40
GRAPEFRUIT SEED OIL
WATER
ISOPROPYL ALCOHOL
ISOPROPYL MYRISTATE
ALOE VERA LEAF
SUNFLOWER SEED
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:50157-115-01 29 mL in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333A 01/10/2015
Labeler — Brands International Corp (243748238)
Establishment
Name Address ID/FEI Operations
Brands International Corp 243748238 manufacture (50157-115)

Revised: 10/2016 Brands International Corp

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Terms of Use | Copyright © 2024. All Rights Reserved.