OTC Medication Information: N69 CUNT

N69 CUNT- alcohol liquid
Guangzhou Oumiao Cosmetics 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.

Active Ingredient

ETHYL ALCOHOL80%

Purpose

Solven

Uses

external usage products, spray on neck , wrist and other surfaces of skin .

Warnings

1.Caution for those who are allergic to ethanol (alcohol).
2.Should be stored in a cool and dry place, away from fire.
3.For external use only.

When using this product, do not use in or near the eyes.
In case of contact, rinse eyes thoroughly with water. Stop use and ask doctor if irritation or rash appears and lasts.

Keep out of reach for children. If swallowed, get medical help or contact a Poison Control Center right away.

do not use in or near the eyes.
In case of contact, rinse eyes thoroughly with water.

When using this product

When using this product, do not use in or near the eyes.
In case of contact, rinse eyes thoroughly with water.

Stop use and ask doctor if irritation or rash appears and lasts.

Keep out of reach for children. If swallowed, get medical help or contact a Poison Control Center right away.

Stop use and ask doctor if irritation or rash appears and lasts.

Keep out of reach for children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Place enough Product in your palm to thoroughly spread on both hands and rub into the skin until dry.
Children under 6 years of age should be supervised when using this product.

Other information

Store below 106°F.(40℃)

Inactive ingredients

AQUA, PARFUM

Package Label — Principal Display Panel

74761-013-01 50ml
(click image for full-size original)

N69 CUNT
n69 cunt liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:74761-017
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALCOHOL (ALCOHOL) ALCOHOL 80 mL in 100 mL
Inactive Ingredients
Ingredient Name Strength
DISPERSE RED 15
WATER
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:74761-017-01 50 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 09/15/2020
Labeler — Guangzhou Oumiao Cosmetics Co. Ltd.  (529806412)
Registrant — Guangzhou Oumiao Cosmetics Co. Ltd.  (529806412)
Establishment
Name Address ID/FEI Operations
Guangzhou Oumiao Cosmetics Co. Ltd.     529806412 manufacture (74761-017)

Revised: 10/2020 Guangzhou Oumiao Cosmetics 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.

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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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