OTC Medication Information: COTTON CANDY SCENTED HAND SANITIZER

COTTON CANDY SCENTED HAND SANITIZER- alcohol solution
Ganzhou Olivee Cosmetic Co., Ltd.

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 ingredient

Alcohol 62%

Purpose

Antiseptic

Use

Decreases bacteria on hands.

Warnings

For external use only.

Flammable. Keep product away from fire or flame.

When using this product

avoid contact with eyes; in case of contact, flush eyes with water.

Stop use and ask a doctor if

irritation or redness develops and persists.

Keep out of reach of children.

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

Directions

Wet hands thoroughly with product and allow to dry.

Inactive ingredients

Water (Aqua), Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Fragrance (Parfum). May Contain: D&C Red No.33 (CI 17200), FD&C Red No.4 (CI 14700), FD&C Yellow No.5 (CI 19140), FD&C Blue No.1 (CI 42090).

OUR POWERFUL GERM-KILLING FORMULA LEAVES HANDS FEELING FRESH AND CLEAN!

Distributed by Best Accessory Group

10 West 37th St. Suite 4E New York NY 10018

Rue de la Victoire 26 Suite: 132494, 1060

Brussels, Belgium

Designed in USA . Made in China

Item#: FB9400AW

WARNING — CHOKING HAZARD

Small Parts. Not for children under 3 years.

NO ANIMAL TESTING.

NEW!

2 in 1

Anti — Bacterial Sanitizer with Holder

www.mybeautyspot.com

Packaging

image description
(click image for full-size original)

COTTON CANDY SCENTED HAND SANITIZER
alcohol solution
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:56136-029
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALCOHOL (ALCOHOL) ALCOHOL 62 mL in 100 mL
Inactive Ingredients
Ingredient Name Strength
WATER
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)
AMINOMETHYLPROPANOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:56136-029-01 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 part333E 03/27/2020
Labeler — Ganzhou Olivee Cosmetic Co., Ltd. (543008195)
Registrant — Ganzhou Olivee Cosmetic Co., Ltd. (543008195)
Establishment
Name Address ID/FEI Operations
Ganzhou Olivee Cosmetic Co., Ltd. 543008195 manufacture (56136-029)

Revised: 03/2020 Ganzhou Olivee Cosmetic Co., Ltd.

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.

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