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NDC 36800-0192-30 All Day Moisture 61.2; 30.6 mg/mL; mg/mL Details

All Day Moisture 61.2; 30.6 mg/mL; mg/mL

All Day Moisture is a TOPICAL LOTION in the HUMAN OTC DRUG category. It is labeled and distributed by Topco. The primary component is OCTINOXATE; ZINC OXIDE.

Product Information

NDC	36800-0192
Product ID	36800-192_c16d0483-552c-41da-8468-94f9ca59029b
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	All Day Moisture
Proprietary Name Suffix	n/a
Non-Proprietary Name	Octinoxate, Zinc Oxide
Product Type	HUMAN OTC DRUG
Dosage Form	LOTION
Route	TOPICAL
Active Ingredient Strength	61.2; 30.6
Active Ingredient Units	mg/mL; mg/mL
Substance Name	OCTINOXATE; ZINC OXIDE
Labeler Name	Topco
Pharmaceutical Class	Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH FINAL
Application Number	part352
Listing Certified Through	2024-12-31

Package

Package Images

NDC 36800-0192-30 (36800019230)

Pricing Information	N/A
NDC Package Code	36800-192-30
Billing NDC	36800019230
Package	1 BOTTLE, PLASTIC in 1 BOX (36800-192-30) / 177 mL in 1 BOTTLE, PLASTIC
Marketing Start Date	2020-02-05
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 9d984b47-0fd2-4177-8f24-50d31c7736ec Details

Active ingredients

Octinoxate 6.0%

Zinc Oxide 3.0%

Purpose

Sunscreen

Uses

helps prevent sunburn
if used as diected with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Warnings

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 use and ask a doctor if

rash occurs

Keep out of reach of children.

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

Directions

apply liberally 15 minutes before sun exposure
reapply at least every 2 hours
use a water resistant sunscreen if swimming or sweating
Sun Protection Measures. spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk regularly use as sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
limit time in the sun, espcially from 10 a.m. - 2 p.m.
wear long-sleeved shirts, pants, hats and sunclasses
children under 6 months of age: ask a doctor

Other information

protect the product from excessive heat and direct sun

Inactive ingredients

water, glycerin, isohexadecane, sodium acrylate/sodium acryloyldimethyl taurate copolymer, polysorbate 80, laureth-7, cylopentasiloxane, cyclohexasiloxane, PEG/PPG-20/20 dimethicone, steareth-21, stearyl alcohol, Gossypium Herbaceum (cotton) seed oil, behenyl alcohol, cetyl alcohol, DMDM hydantoin, iodopropynyl butylcarbamate, fragrance, tocopheryl acetate, disodium EDTA, steareth-2, oleth-3 phosphate, ascorbic acid, panthenol

claims

TopCare

beauty

ALL-DAY

MOISTURE LOTION

For Normal Skin

Light, non-greasyt formula

Non-comedogenic

(won't clog pores)

Paraben Free

Light, fast-absorbing

moisture lasts all day

Softens

Smoothes for radiant skin

ALL-DAY

MOISTURE LOTION

For Normal Skin

ALL DAY MOISTURE

Complete beauty lotion moisture for all day hydration.

Formulated antioxidant vitamin E plus C and nourishing beauty moisture that absorbs quickly into skin and lasts all day to help your skin stay soft, smooth and beautiful

UV PROTECTION

Broad spectrum

UVA and UVB protection with SPF 15 to help prevent premature skin damage.

SPL UNCLASSIFIED SECTION

DISTRIBUTED BY TOPCO ASSOCIATES LLC

ELK GROVE VILLAGE, IL 60007

TOPCO VIJA1019

QUESTIONS? 1-888-420139

This product is not manufactured or distributed by Procter & Gamble, distributor of Olay Complete All Day Moisturizer with Sunscreen.

principal display panel

TopCare

beauty

ALL-DAY

MOISTURE LOTION

For Normal Skin

Compare to OLAY

Broad spectrum SPF 15 sunscreen

Dermatologist Tested

SPF 15

6 FL OZ (177mL)

INGREDIENTS AND APPEARANCE

ALL DAY MOISTURE

octinoxate, zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:36800-192
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
Octinoxate (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	Octinoxate	61.2 mg in 1 mL
Zinc Oxide (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	30.6 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
Water (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ISOHEXADECANE (UNII: 918X1OUF1E)
SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
LAURETH-7 (UNII: Z95S6G8201)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
PEG/PPG-20/20 DIMETHICONE (UNII: BA94B7CK8K)
STEARETH-21 (UNII: 53J3F32P58)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
LEVANT COTTONSEED OIL (UNII: N5CFT140R8)
DOCOSANOL (UNII: 9G1OE216XY)
CETYL ALCOHOL (UNII: 936JST6JCN)
DMDM HYDANTOIN (UNII: BYR0546TOW)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
EDETATE DISODIUM (UNII: 7FLD91C86K)
STEARETH-2 (UNII: V56DFE46J5)
OLETH-3 PHOSPHATE (UNII: 8Q0Z18J1VL)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
PANTHENOL (UNII: WV9CM0O67Z)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:36800-192-30	1 in 1 BOX	02/05/2020
1		177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part352	02/05/2020

Labeler - Topco (006935977)

Registrant - Vi-Jon, LLC (790752542)

Name	Address	ID/FEI	Business Operations
Establishment
Vi-Jon, LLC		790752542	manufacture(36800-192)

Name	Address	ID/FEI	Business Operations
Establishment
Vi-Jon, LLC		088520668	manufacture(36800-192)

Revised: 4/2022

Document Id: c16d0483-552c-41da-8468-94f9ca59029b

Set id: 9d984b47-0fd2-4177-8f24-50d31c7736ec

Version: 7

Effective Time: 20220411

Search by Drug Name or NDC

NDC 36800-0192-30 All Day Moisture 61.2; 30.6 mg/mL; mg/mL Details

All Day Moisture 61.2; 30.6 mg/mL; mg/mL

Product Information

Package

Package Images

NDC 36800-0192-30 (36800019230)

Contents

Standard Product Labeling (SPL)/Prescribing Information SPL 9d984b47-0fd2-4177-8f24-50d31c7736ec Details

Active ingredients

Purpose

Uses

Warnings

Do not use

When using this product

Stop use and ask a doctor if

Keep out of reach of children.

Directions

Other information

Inactive ingredients

claims

SPL UNCLASSIFIED SECTION

principal display panel

INGREDIENTS AND APPEARANCE

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