NDC | 69774-551-02 |
Set ID | 4a1faf2b-bf8c-3249-e054-00144ff8d46c |
Category | HUMAN OTC DRUG LABEL |
Packager | SKIN SCIENCES LABORATORY INC. |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART333D |
- ACTIVE INGREDIENT
- PURPOSE
- WARNINGS
-
WHEN USING
When using this product
- Apply to affected areas only
- Avoid unnecessary sun exposure and use a sunscreen
- Do not use in or near the eyes
- Using other topical acne drugs at the same time
or right after use of this product
may increase dryness or irritation of the skin.
Only one drug should be used unless directed by a doctor - KEEP OUT OF REACH OF CHILDREN
-
DOSAGE & ADMINISTRATION
Directions
- 2x-a-day, massage a small
amount onto wet skin. Rinse well.
- Because excessive drying of the
skin may occur, start with one
application daily, then gradually
increase to two or three times daily
if needed or as directed by a doctor
- If bothersome dryness or peeling occurs,
reduce application to once a day or every other day. -
STORAGE AND HANDLING
Other information
- Protect the product in this container from excessive heat and direct sun.
- Before use, test a tiny amount on skin (we omit allergens, but you may be sensitive
to an ingredient that is not an allergen.
- Introduce new skin products one at a time, with at least 3 days in between.
- Do not (re)introduce removed portions of product or other substances into container. -
INACTIVE INGREDIENT
Inactive ingredients
Aqua/Water/Eau, Butylene Glycol,
Camellia Sinensis Leaf Extract,
Caprylyl Glycol, Cocos Nucifera (Coconut) Oil
Disodium Laureth Sulfosuccinate, Glycerin, Glyceryl Laurate,
Glyceryl Stearate, 1,2-Hexanediol, Paraffin, Pumice
Sodium Laureth Sulfate, Sodium Phytate, Stearic Acid, Stearyl Alcohol -
OTHER SAFETY INFORMATION
Notes: If contact with eyes
occurs, flush out with plenty of
water. This product is meant to be washed off quickly, not left on the
skin for longer than a few seconds
while cleansing. Prolonged
exposure without rinsing
immediately may cause irritation to
skin. Stop use and consult your
doctor in the unlikely event of
discomfort or sensitivity. 1ST-TIME
USERS: Some first-time users may
experience an initial acne
break-out due to the deeper
exfoliation of the pores' inner
walls. If your pores have not been
regularly cleaned at this level,
existing pore cloggers are brought
to the surface. As therapy
continues, this deeper-cleaned
state is maintained and acne is
markedly reduced. With correct
use - following instructions
carefully, the slow increase in
application frequency, the use of
hypoallergenic, non-comedogenic
and pH-appropriate support
products in the Id system - as well
as prevention with non-comedo-
genic products such as Essence
Skin-Saving Hair, Body + Bath Care,
Armada Sun + Light Screens,
Skintelligent Beauty Makeup, this
initial reaction soon disappears. If it
does occur, stop use for 1 week
and restart therapy at the
beginning, with 2x-a-week
applications. CYSTIC ACNE can
be internally caused. If you have
cystic acne, consult your
dermatologist as you may need
additional medication and/or other
management. - CLINICAL STUDIES
- INDICATIONS & USAGE
-
PRINCIPAL DISPLAY PANEL
id
SKIN-BUFFING
CLEANSING SCRUBcleansing
for treated skinmild, pH-adjusted, gently
exfoliating cleanser for
skin undergoing active
treatmentsclarifying, smoothening +
exfoliating systemValidated
Hypoallergenic:
VH -109/109
sans all common allergens,
extended allergen series:
North American Contact Dermatitis
Group + European Surveillance
System on Contact Allergies100% All-Types-Of-Fragrance-Free.
100% SLS + Allergen-Surfactant-Free.
100% Dye, Phthalate, Paraben + Preservative-Free.
Usage + Patch Tested.
Non-Comedogenic. Non-Drying.
For All Skin Types.
For Men + Women.
120 mL (4 Fl. Oz.) - 120 mL
-
INGREDIENTS AND APPEARANCE
VMV HYPOALLERGENICS ID SKIN-BUFFING CLEANSING SCRUB
salicylic acid emulsionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69774-551 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 1.2 g in 120 mL Inactive Ingredients Ingredient Name Strength 1,2-HEXANEDIOL (UNII: TR046Y3K1G) GLYCERIN (UNII: PDC6A3C0OX) 12-(9-ANTHROYLOXY)STEARIC ACID (UNII: 039Y7Q32CO) GLYCERYL LAURATE (UNII: Y98611C087) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) CAPRYLYL GLYCOL (UNII: 00YIU5438U) DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) WATER (UNII: 059QF0KO0R) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) PARAFFIN (UNII: I9O0E3H2ZE) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) PHYTATE SODIUM (UNII: 88496G1ERL) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69774-551-02 1 in 1 BOX 05/15/2017 1 120 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 05/15/2017 Labeler - SKIN SCIENCES LABORATORY INC. (718777360) Establishment Name Address ID/FEI Business Operations SKIN PRESCRIPTIVES MARKETING, INC. 718955750 manufacture(69774-551)