OTC Medication Information: ELF Perm

ELF PERM- panthenol cream
giod Co.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Panthenol 0.1%

Hair Perm

Shampoo and remove excessive moisture from hair with a towel
Apply the first solution and roll hair in curlers
Allow 10 minutes of heat treatment (Adjust ±5-10 minutes depends on the time needed)
Apply second solution and rinse

Shampoo and remove excessive moisture from hair with a towel
Apply the first solution and roll hair in curlers
Allow 10 minutes of heat treatment (Adjust ±5-10 minutes depends on the time needed)
Apply second solution and rinse

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 using and ask a doctor if rash occurs.

Keep out of reach of the children. If product is swallowed, get medical help or contact a poison control center right away.

Propylene Glycol, Cysteamine HCl, Ethanolamine Thioglycolate, Ethanolamine, Hydrolyzed Collagen, Cetrimonium Chloride, Glycine, Sodium Carbonate, Algin, Cellulose Gum, Glutamine, Disodium EDTA, Glycerin, Alcohol, Scutellaria Baicalensis Root Extract, Camellia Sinensis Leaf Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Water

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ELF PERM
panthenol cream
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:70072-003
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PANTHENOL (PANTHENOL) PANTHENOL 0.47 g in 479.39 g
Inactive Ingredients
Ingredient Name Strength
PROPYLENE GLYCOL
CYSTEAMINE HYDROCHLORIDE
MONOETHANOLAMINE THIOGLYCOLATE
MONOETHANOLAMINE
CETRIMONIUM CHLORIDE
GLYCINE
SODIUM CARBONATE
SODIUM ALGINATE
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM
GLUTAMINE
EDETATE DISODIUM
GLYCERIN
ALCOHOL
SCUTELLARIA BAICALENSIS ROOT
GREEN TEA LEAF
GLYCYRRHIZA GLABRA
WATER
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:70072-003-02 1 CONTAINER in 1 CARTON contains a CONTAINER (70072-003-01)
1 NDC:70072-003-01 479.39 g in 1 CONTAINER This package is contained within the CARTON (70072-003-02)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 09/05/2015
Labeler — giod Co. (689514993)
Registrant — giod Co. (689514993)
Establishment
Name Address ID/FEI Operations
giod Co. 689514993 manufacture (70072-003)

Revised: 09/2015 giod Co.

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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